C07C47/20

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##

Hydroformylated Triglycerides and Uses Thereof
20210230651 · 2021-07-29 ·

This disclosure provides methods for the chemical modification of triglycerides that are highly enriched in specific fatty acids and subsequent use thereof for producing functionally versatile polymers.

Process for preparing 4-penten-2-ynal

A process for preparing 4-penten-2-ynal of the following formula (2):
CH.sub.2═CHC≡CCHO  (2)
the process comprising a step of hydrolyzing a 5,5-dialkoxy-1-penten-3-yne compound of the following general formula (1):
CH.sub.2═CHC≡CCH(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,
to obtain 4-penten-2-ynal (2). ##STR00001##

Process for preparing 4-penten-2-ynal

A process for preparing 4-penten-2-ynal of the following formula (2):
CH.sub.2═CHC≡CCHO  (2)
the process comprising a step of hydrolyzing a 5,5-dialkoxy-1-penten-3-yne compound of the following general formula (1):
CH.sub.2═CHC≡CCH(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,
to obtain 4-penten-2-ynal (2). ##STR00001##

PROCESS FOR PREPARING 4-PENTEN-2-YNAL
20210061745 · 2021-03-04 ·

A process for preparing 4-penten-2-ynal of the following formula (2):


CH.sub.2CHCCCHO(2)

the process comprising a step of hydrolyzing a 5,5-dialkoxy-1-penten-3-yne compound of the following general formula (1):


CH.sub.2CHCCCH(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,
to obtain 4-penten-2-ynal (2).

##STR00001##

PROCESS FOR PREPARING 4-PENTEN-2-YNAL
20210061745 · 2021-03-04 ·

A process for preparing 4-penten-2-ynal of the following formula (2):


CH.sub.2CHCCCHO(2)

the process comprising a step of hydrolyzing a 5,5-dialkoxy-1-penten-3-yne compound of the following general formula (1):


CH.sub.2CHCCCH(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,
to obtain 4-penten-2-ynal (2).

##STR00001##

DIALKOXYALKADIENYNE COMPOUND AND A PROCESS FOR PREPARING THE SAME AND A PROCESS FOR PREPARING A DIENYNAL COMPOUND
20210061744 · 2021-03-04 ·

A process for preparing a dienynal compound of the following general formula (2): CH.sub.2CHCCCHCH(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.2CHCCCHCH(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, mere 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##

DIALKOXYALKADIENYNE COMPOUND AND A PROCESS FOR PREPARING THE SAME AND A PROCESS FOR PREPARING A DIENYNAL COMPOUND
20210061744 · 2021-03-04 ·

A process for preparing a dienynal compound of the following general formula (2): CH.sub.2CHCCCHCH(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.2CHCCCHCH(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, mere 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##

HYDROFORMYLATED TRIGLYCERIDES AND USES THEREOF
20240124378 · 2024-04-18 ·

This disclosure provides methods for the chemical modification of triglycerides that are highly enriched in specific fatty acids and subsequent use thereof for producing functionally versatile polymers.

HYDROFORMYLATED TRIGLYCERIDES AND USES THEREOF
20240124378 · 2024-04-18 ·

This disclosure provides methods for the chemical modification of triglycerides that are highly enriched in specific fatty acids and subsequent use thereof for producing functionally versatile polymers.