C07C43/15

POLYALKYLENE GLYCOL COMPOUND
20220081513 · 2022-03-17 · ·

A polyalkylene glycol-based compound of formula (1):

##STR00001##

may be one in which R.sup.1 is a monovalent hydrocarbon group having 1 to 32 carbon atoms, a monovalent aromatic hydrocarbon group having 6 to 42 ring carbon atoms, a monovalent acyl group having 2 to 32 carbon atoms, or a monovalent oxygen-containing hydrocarbon group having 2 to 32 carbon atoms; R.sup.2 is a monovalent hydrocarbon group having 1 to 32 carbon atoms, a monovalent aromatic hydrocarbon group having 6 to 42 ring carbon atoms, a monovalent acyl group having 2 to 32 carbon atoms, a monovalent oxygen-containing hydrocarbon group having 2 to 32 carbon atoms, or a hydrogen atom; R.sup.3 is a divalent hydrocarbon group having 4 carbon atoms; R.sup.4 is a divalent hydrocarbon group having 2 or 3 carbon atoms; m and n are respectively numbers between 1 and 40 and 0 and 20; and m/(m+n)≥0.5.

POLYALKYLENE GLYCOL COMPOUND
20220081513 · 2022-03-17 · ·

A polyalkylene glycol-based compound of formula (1):

##STR00001##

may be one in which R.sup.1 is a monovalent hydrocarbon group having 1 to 32 carbon atoms, a monovalent aromatic hydrocarbon group having 6 to 42 ring carbon atoms, a monovalent acyl group having 2 to 32 carbon atoms, or a monovalent oxygen-containing hydrocarbon group having 2 to 32 carbon atoms; R.sup.2 is a monovalent hydrocarbon group having 1 to 32 carbon atoms, a monovalent aromatic hydrocarbon group having 6 to 42 ring carbon atoms, a monovalent acyl group having 2 to 32 carbon atoms, a monovalent oxygen-containing hydrocarbon group having 2 to 32 carbon atoms, or a hydrogen atom; R.sup.3 is a divalent hydrocarbon group having 4 carbon atoms; R.sup.4 is a divalent hydrocarbon group having 2 or 3 carbon atoms; m and n are respectively numbers between 1 and 40 and 0 and 20; and m/(m+n)≥0.5.

HALOALKENYL ALKOXYMETHYL ETHER COMPOUND AND A PROCESS FOR PREPARING A TERMINAL CONJUGATED ALKADIEN-1-YL ACETATE COMPOUND AND A TERMINAL CONJUGATED ALKADIEN-1-OL COMPOUND THEREFROM
20220106253 · 2022-04-07 ·

The present invention relates to a haloalkenyl 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.aX.sup.1 (1) wherein R.sup.1 represents a hydrogen atom, an n-alkyl group having 1 to 9 carbon atoms, or a phenyl group, X.sup.1 represents a halogen atom, and “a” represents an integer of 3 to 14. The present invention also relates to processes for preparing a terminal conjugated alkadien-1-yl acetate compound of the following general formula (5): CH.sub.2═CHCH═CH(CH.sub.2).sub.aOAc (5) wherein “a” is as defined above, and Ac represents an acetyl group, and a terminal conjugated alkadien-1-ol compound of the following general formula (6): CH.sub.2═CHCH═CH(CH.sub.2).sub.aOH (6) wherein “a” is as defined above, from the haloalkenyl alkoxymethyl ether compound (1).

HALOALKENYL ALKOXYMETHYL ETHER COMPOUND AND A PROCESS FOR PREPARING A TERMINAL CONJUGATED ALKADIEN-1-YL ACETATE COMPOUND AND A TERMINAL CONJUGATED ALKADIEN-1-OL COMPOUND THEREFROM
20220106253 · 2022-04-07 ·

The present invention relates to a haloalkenyl 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.aX.sup.1 (1) wherein R.sup.1 represents a hydrogen atom, an n-alkyl group having 1 to 9 carbon atoms, or a phenyl group, X.sup.1 represents a halogen atom, and “a” represents an integer of 3 to 14. The present invention also relates to processes for preparing a terminal conjugated alkadien-1-yl acetate compound of the following general formula (5): CH.sub.2═CHCH═CH(CH.sub.2).sub.aOAc (5) wherein “a” is as defined above, and Ac represents an acetyl group, and a terminal conjugated alkadien-1-ol compound of the following general formula (6): CH.sub.2═CHCH═CH(CH.sub.2).sub.aOH (6) wherein “a” is as defined above, from the haloalkenyl alkoxymethyl ether compound (1).

Wax Ethers and Related Methods
20210317056 · 2021-10-14 ·

Implementations of a method of forming a wax ether composition may include: providing a batch of lipids, drying the batch of lipids, and cooling the batch of lipids. The method may also include dosing, with a catalyst, the batch of lipids at 0.1% to 0.3% by weight of the batch of lipids and dissolving the catalyst in the batch of lipids to form a homogenous solution. The method may include adding at least a molar equivalent of a hydrogen donor to the homogenous solution. The method may include sealing and maintaining the homogenous solution and hydrogen donor under atmospheric pressure under reflux until a chemical reaction between the homogenous solution and the hydrogen donor forms a product comprising an ether.

Wax Ethers and Related Methods
20210317056 · 2021-10-14 ·

Implementations of a method of forming a wax ether composition may include: providing a batch of lipids, drying the batch of lipids, and cooling the batch of lipids. The method may also include dosing, with a catalyst, the batch of lipids at 0.1% to 0.3% by weight of the batch of lipids and dissolving the catalyst in the batch of lipids to form a homogenous solution. The method may include adding at least a molar equivalent of a hydrogen donor to the homogenous solution. The method may include sealing and maintaining the homogenous solution and hydrogen donor under atmospheric pressure under reflux until a chemical reaction between the homogenous solution and the hydrogen donor forms a product comprising an ether.

ESTERS AND ETHERS OF 3-METHYL-PENTANE-DIOL AND UNSATURATED DERIVATIVES THEREOF AND THEIR USE AS AROMA CHEMICAL
20210228459 · 2021-07-29 ·

The present invention relates to the use of esters and/or ethers of 3-methyl-pentane-diol and unsaturated derivates thereof as aroma chemicals, to aroma chemical compositions comprising at least one ester of 3-methyl-pentan-diol and/or unsaturated derivates thereof and/or at least one ether of 3-methyl-pentan-diol and/or unsaturated derivates thereof and to a method for preparing an aroma chemical composition, in particular a fragranced composition, specifically a fragranced ready-to-use composition, which comprises incorporating at least one ester of 3-methyl-pentane-diol and/or one or more unsaturated derivates thereof and/or at least one ether 3-methyl-pentane-diol and/or one or more unsaturated derivates thereof into a composition, in particular into a ready-to-use composition. The present invention further relates to specific ethers of 3-methyl-pentane-diol and unsaturated derivates thereof and to specific esters of 3-methyl-pentane-diol, to specific mixtures of such compounds and to unsaturated derivates thereof and a method for their preparation.

Compositions comprising odorants

The present invention relates to odorous 2- and/or 3-substituted 3-(allyloxy)propenes which are useful as fragrance or flavor ingredients in particular in providing green, fruity, pear and/or waxy olfactory notes. The present invention also relates to novel perfume, aroma or deodorizing/masking compositions comprising said odorants.

Compositions comprising odorants

The present invention relates to odorous 2- and/or 3-substituted 3-(allyloxy)propenes which are useful as fragrance or flavor ingredients in particular in providing green, fruity, pear and/or waxy olfactory notes. The present invention also relates to novel perfume, aroma or deodorizing/masking compositions comprising said odorants.

Compositions comprising odorants

The present invention relates to odorous 2- and/or 3-substituted 3-(allyloxy)propenes which are useful as fragrance or flavor ingredients in particular in providing green, fruity, pear and/or waxy olfactory notes. The present invention also relates to novel perfume, aroma or deodorizing/masking compositions comprising said odorants.