2-[((E)-Hex-2-enyl)oxy]-3-hydroxy-3-methyl-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester

Base Information

Chemical Name:2-[((E)-Hex-2-enyl)oxy]-3-hydroxy-3-methyl-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester
CAS No.:256416-34-9
Molecular Formula:C₂₁H₃₈O₄
Molecular Weight:354.53
Hs Code.:

Synonyms:2-[((E)-Hex-2-enyl)oxy]-3-hydroxy-3-methyl-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester

Suppliers and Price of 2-[((E)-Hex-2-enyl)oxy]-3-hydroxy-3-methyl-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-[((E)-Hex-2-enyl)oxy]-3-hydroxy-3-methyl-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-[((E)-Hex-2-enyl)oxy]-3-hydroxy-3-methyl-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester

There total 3 articles about 2-[((E)-Hex-2-enyl)oxy]-3-hydroxy-3-methyl-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 74.0%

: 67-64-1
acetone

: 256416-30-5
[((E)-Hex-2-enyl)oxy]-acetic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester

: 256416-34-9
2-[((E)-Hex-2-enyl)oxy]-3-hydroxy-3-methyl-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; at -78 ℃; for 0.5h;
DOI:10.1002/(SICI)1099-0690(199911)1999:11<2713::AID-EJOC2713>3.0.CO;2-E

Reference yield:

: 2216-51-5
(-)-menthol

: 256416-34-9
2-[((E)-Hex-2-enyl)oxy]-3-hydroxy-3-methyl-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / DCC / DMAP / CH₂Cl₂ / 0 °C

2: 74 percent / LDA / tetrahydrofuran / 0.5 h / -78 °C

With dicyclohexyl-carbodiimide; lithium diisopropyl amide; dmap; In tetrahydrofuran; dichloromethane; 1: Esterification / 2: Aldol addition;
DOI:10.1002/(SICI)1099-0690(199911)1999:11<2713::AID-EJOC2713>3.0.CO;2-E

Reference yield:

: 175019-14-4
(E)-2-(hex-2-en-1-yloxy)acetic acid

: 256416-34-9
2-[((E)-Hex-2-enyl)oxy]-3-hydroxy-3-methyl-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / DCC / DMAP / CH₂Cl₂ / 0 °C

2: 74 percent / LDA / tetrahydrofuran / 0.5 h / -78 °C

With dicyclohexyl-carbodiimide; lithium diisopropyl amide; dmap; In tetrahydrofuran; dichloromethane; 1: Esterification / 2: Aldol addition;
DOI:10.1002/(SICI)1099-0690(199911)1999:11<2713::AID-EJOC2713>3.0.CO;2-E