((2S,3R,6R)-1-Hydroxy-3-isopropenyl-2,6-dimethyl-cyclohexyl)-acetic acid ethyl ester

Base Information

Chemical Name:((2S,3R,6R)-1-Hydroxy-3-isopropenyl-2,6-dimethyl-cyclohexyl)-acetic acid ethyl ester
CAS No.:331961-16-1
Molecular Formula:C₁₅H₂₆O₃
Molecular Weight:254.37
Hs Code.:

Synonyms:((2S,3R,6R)-1-Hydroxy-3-isopropenyl-2,6-dimethyl-cyclohexyl)-acetic acid ethyl ester

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Chemical Property of ((2S,3R,6R)-1-Hydroxy-3-isopropenyl-2,6-dimethyl-cyclohexyl)-acetic acid ethyl ester

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Technology Process of ((2S,3R,6R)-1-Hydroxy-3-isopropenyl-2,6-dimethyl-cyclohexyl)-acetic acid ethyl ester

There total 2 articles about ((2S,3R,6R)-1-Hydroxy-3-isopropenyl-2,6-dimethyl-cyclohexyl)-acetic acid ethyl 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: 48.0%

: 927-80-0
1-ethoxyacetylene

: 331961-14-9
(2S,3R,6R)-2,6-dimethyl-3-(prop-1-en-2-yl)cyclohexan-1-one

: 331961-15-0
Ethyl [(2S,3R,6R)-2,6-dimethyl-3-isopropenylcyclohexylidene]acetate

: 331961-16-1
((2S,3R,6R)-1-Hydroxy-3-isopropenyl-2,6-dimethyl-cyclohexyl)-acetic acid ethyl ester

Guidance literature:: 1-ethoxyacetylene; With ethylmagnesium bromide; In tetrahydrofuran; toluene; at 0 - 60 ℃;

(2S,3R,6R)-2,6-dimethyl-3-(prop-1-en-2-yl)cyclohexan-1-one; In tetrahydrofuran; toluene; for 2h; Heating;

With sulfuric acid; In tetrahydrofuran; for 10h; Further stages.;
DOI:10.1002/1521-3765(20010119)7:2<520::AID-CHEM520>3.0.CO;2-5

Reference yield:

: 91781-46-3
(6S,5R)-2,6-dimethyl-5-(1-methylethenyl)-2-cyclohexen-1-one

: 331961-16-1
((2S,3R,6R)-1-Hydroxy-3-isopropenyl-2,6-dimethyl-cyclohexyl)-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: 80 percent / aq. NaHCO₃; sodium dithionite / Adogen 464 / toluene / 2 h / Heating

2.1: EtMgBr / toluene; tetrahydrofuran / 0 - 60 °C

2.2: toluene; tetrahydrofuran / 2 h / Heating

2.3: 48 percent / aq. H₂SO₄ / tetrahydrofuran / 10 h

With sodium dithionite; ethylmagnesium bromide; sodium hydrogencarbonate; adogen 464; In tetrahydrofuran; toluene;
DOI:10.1002/1521-3765(20010119)7:2<520::AID-CHEM520>3.0.CO;2-5

Reference yield: 71.0%

: 75-36-5
acetyl chloride

: 331961-16-1
((2S,3R,6R)-1-Hydroxy-3-isopropenyl-2,6-dimethyl-cyclohexyl)-acetic acid ethyl ester

: 331961-17-2
((2S,3R,6R)-1-Acetoxy-3-isopropenyl-2,6-dimethyl-cyclohexyl)-acetic acid ethyl ester

Guidance literature:: With N,N-dimethyl-aniline; In chloroform; for 24h; Heating;
DOI:10.1002/1521-3765(20010119)7:2<520::AID-CHEM520>3.0.CO;2-5