Patent classifications
C07C45/515
7-methyl-3-methylene-7-octenal acetal compound and methods for producing aldehyde compound and ester compound using the same
There are provided methods of efficiently producing compounds that are, for example, sex pheromones of San Jose Scale. For example, there is provided a method for producing a 7-methyl-3-methylene-7-octenyl carboxylate compound (4), the method including the steps of: hydrolyzing a 7-methyl-3-methylene-7-octenal acetal compound (1) to obtain 7-methyl-3-methylene-7-octenal (2); reducing the 7-methyl-3-methylene-7-octenal (2) to obtain 7-methyl-3-methylene-7-octenol (3); and esterifying the 7-methyl-3-methylene-7-octenol (3) to obtain a 7-methyl-3-methylene-7-octenyl carboxylate compound (4). ##STR00001##
Dialkoxyalkenyl alkoxymethyl ether compound and a process for preparing a terminal conjugated alkadienal compound from the same
The present invention provides a process for preparing a terminal conjugated alkadienal compound of the following general formula (5):
CH.sub.2═CHCH═CH(CH.sub.2).sub.aCHO (5)
wherein “a” represents an integer of 1 to 15, from a dialkoxyalkenyl alkoxymethyl ether compound of the following general formula (1):
R.sup.1CH.sub.2OCH.sub.2OCH.sub.2CH.sub.2CH═CH(CH.sub.2).sub.aCH(OR.sup.2)(OR.sup.3) (1)
wherein R.sup.1 represents a hydrogen atom, an n-alkyl group having 1 to 9 carbon atoms, or a phenyl group, R.sup.2 and R.sup.3 represent, independently of each other, a monovalent hydrocarbon group having 1 to 15 carbon atoms, or R.sup.2 and R.sup.3 may form together a divalent hydrocarbon group, R.sup.2-R.sup.3, having 2 to 10 carbon atoms, and “a” is as defined above.
Dialkoxyalkenyl alkoxymethyl ether compound and a process for preparing a terminal conjugated alkadienal compound from the same
The present invention provides a process for preparing a terminal conjugated alkadienal compound of the following general formula (5):
CH.sub.2═CHCH═CH(CH.sub.2).sub.aCHO (5)
wherein “a” represents an integer of 1 to 15, from a dialkoxyalkenyl alkoxymethyl ether compound of the following general formula (1):
R.sup.1CH.sub.2OCH.sub.2OCH.sub.2CH.sub.2CH═CH(CH.sub.2).sub.aCH(OR.sup.2)(OR.sup.3) (1)
wherein R.sup.1 represents a hydrogen atom, an n-alkyl group having 1 to 9 carbon atoms, or a phenyl group, R.sup.2 and R.sup.3 represent, independently of each other, a monovalent hydrocarbon group having 1 to 15 carbon atoms, or R.sup.2 and R.sup.3 may form together a divalent hydrocarbon group, R.sup.2-R.sup.3, having 2 to 10 carbon atoms, and “a” is as defined above.
Process for preparing a formylalkenyl alkoxymethyl ether compound and processes for preparing conjugated diene compounds from the same
The present invention provide for preparing a formylalkenyl alkoxymethyl ether compound of the following general formula (2): R.sup.3CH.sub.2OCH.sub.2O(CH.sub.2).sub.aCH═CHCHO (2), wherein R.sup.3 represents a hydrogen atom, an n-alkyl group having 1 to 9 carbon atoms, or a phenyl group; and “a” represents an integer of 1 to 10, the process comprising: hydrolyzing a dialkoxyalkenyl alkoxymethyl ether compound of the following general formula (1): R.sup.3CH.sub.2OCH.sub.2O(CH.sub.2).sub.aCH═CHCH(OR.sup.1)(OR.sup.2) (1), wherein R.sup.1 and R.sup.2 represent, independently of each other, a monovalent hydrocarbon group having 1 to 15 carbon atoms, or R.sup.1 and R.sup.2 may form together a divalent hydrocarbon group, R.sup.1-R.sup.2, having 2 to 10 carbon atoms; and R.sup.3 and “a” are as defined above, in the presence of an acid while removing an alcohol compound thus generated to form the formylalkenyl alkoxymethyl ether compound (2).
Process for preparing a formylalkenyl alkoxymethyl ether compound and processes for preparing conjugated diene compounds from the same
The present invention provide for preparing a formylalkenyl alkoxymethyl ether compound of the following general formula (2): R.sup.3CH.sub.2OCH.sub.2O(CH.sub.2).sub.aCH═CHCHO (2), wherein R.sup.3 represents a hydrogen atom, an n-alkyl group having 1 to 9 carbon atoms, or a phenyl group; and “a” represents an integer of 1 to 10, the process comprising: hydrolyzing a dialkoxyalkenyl alkoxymethyl ether compound of the following general formula (1): R.sup.3CH.sub.2OCH.sub.2O(CH.sub.2).sub.aCH═CHCH(OR.sup.1)(OR.sup.2) (1), wherein R.sup.1 and R.sup.2 represent, independently of each other, a monovalent hydrocarbon group having 1 to 15 carbon atoms, or R.sup.1 and R.sup.2 may form together a divalent hydrocarbon group, R.sup.1-R.sup.2, having 2 to 10 carbon atoms; and R.sup.3 and “a” are as defined above, in the presence of an acid while removing an alcohol compound thus generated to form the formylalkenyl alkoxymethyl ether compound (2).
DIALKOXYALKENYL ALKOXYMETHYL ETHER COMPOUND AND A PROCESS FOR PREPARING A TERMINAL CONJUGATED ALKADIENAL COMPOUND FROM THE SAME
The present invention provides a process for preparing a terminal conjugated alkadienal compound of the following general formula (5):
CH.sub.2═CHCH═CH(CH.sub.2).sub.aCHO (5)
wherein “a” represents an integer of 1 to 15, from a dialkoxyalkenyl alkoxymethyl ether compound of the following general formula (1):
R.sup.1CH.sub.2OCH.sub.2OCH.sub.2CH.sub.2CH═CH(CH.sub.2).sub.aCH(OR.sup.2)(OR.sup.3) (1)
wherein R.sup.1 represents a hydrogen atom, an n-alkyl group having 1 to 9 carbon atoms, or a phenyl group, R.sup.2 and R.sup.3 represent, independently of each other, a monovalent hydrocarbon group having 1 to 15 carbon atoms, or R.sup.2 and R.sup.3 may form together a divalent hydrocarbon group, R.sup.2-R.sup.3, having 2 to 10 carbon atoms, and “a” is as defined above.
DIALKOXYALKENYL ALKOXYMETHYL ETHER COMPOUND AND A PROCESS FOR PREPARING A TERMINAL CONJUGATED ALKADIENAL COMPOUND FROM THE SAME
The present invention provides a process for preparing a terminal conjugated alkadienal compound of the following general formula (5):
CH.sub.2═CHCH═CH(CH.sub.2).sub.aCHO (5)
wherein “a” represents an integer of 1 to 15, from a dialkoxyalkenyl alkoxymethyl ether compound of the following general formula (1):
R.sup.1CH.sub.2OCH.sub.2OCH.sub.2CH.sub.2CH═CH(CH.sub.2).sub.aCH(OR.sup.2)(OR.sup.3) (1)
wherein R.sup.1 represents a hydrogen atom, an n-alkyl group having 1 to 9 carbon atoms, or a phenyl group, R.sup.2 and R.sup.3 represent, independently of each other, a monovalent hydrocarbon group having 1 to 15 carbon atoms, or R.sup.2 and R.sup.3 may form together a divalent hydrocarbon group, R.sup.2-R.sup.3, having 2 to 10 carbon atoms, and “a” is as defined above.
SYNTHESIS OF COELENTERAZINE SYNTHESIS INTERMEDIATE
Disclosed herein are synthesis methods for coelenterazine and intermediates. Also disclosed are articles including the coelenterazine and coelenterazine derivatives. Representative absorbent articles include disposable diapers and adult incontinence products.
SYNTHESIS OF COELENTERAZINE SYNTHESIS INTERMEDIATE
Disclosed herein are synthesis methods for coelenterazine and intermediates. Also disclosed are articles including the coelenterazine and coelenterazine derivatives. Representative absorbent articles include disposable diapers and adult incontinence products.
Dialkoxyalkadienyne compound and a process for preparing the same and a process for preparing a dienynal compound
A process for preparing a dienynal compound of the following general formula (2):
CH.sub.2═CHC≡CCH═CH(CH.sub.2).sub.nCHO (2), wherein n represents an integer of 0 to 11, the process comprising a step of hydrolyzing a dialkoxyalkadienyne compound of the following general formula (1):
CH.sub.2═CHC≡CCH═CH(CH.sub.2).sub.nCH(OR.sup.1)(OR.sup.2) (1) wherein R.sup.1 and R.sup.2 represent, independently of each other, a monovalent hydrocarbon group having 1 to 15 carbon atoms, preferably 1 to 8, more preferably 1 to 4, or R.sup.1 and R.sup.2 may be bonded to each other to form a divalent hydrocarbon group, R.sup.1-R.sup.2, having from 2 to 10 carbon atoms, and n represents an integer of 0 to 11, to obtain the dienynal compound (2). ##STR00001##