methyl 4-[(1S,2S)-2-hydroxy-2,6,6-trimethylcyclohexyl]butanoate

Base Information

• Chemical Name: methyl 4-[(1S,2S)-2-hydroxy-2,6,6-trimethylcyclohexyl]butanoate
• CAS No.: 680218-11-5
• Molecular Formula: C₁₄H₂₆O₃
• Molecular Weight: 242.359
• Mol file: 680218-11-5.mol

Synonyms:methyl 4-[(1S,2S)-2-hydroxy-2,6,6-trimethylcyclohexyl]butanoate

Chemical Property of methyl 4-[(1S,2S)-2-hydroxy-2,6,6-trimethylcyclohexyl]butanoate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of methyl 4-[(1S,2S)-2-hydroxy-2,6,6-trimethylcyclohexyl]butanoate

There total 4 articles about methyl 4-[(1S,2S)-2-hydroxy-2,6,6-trimethylcyclohexyl]butanoate 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: 96.0%

methanol (67-56-1) + (1S,7S)-1,8,8-trimethyl-2-oxabicyclo[5.4.0]undecan-3-one (217467-50-0) → methyl 4-[(1S,2S)-2-hydroxy-2,6,6-trimethylcyclohexyl]butanoate (680218-11-5)

Guidance literature:

With potassium carbonate; at 25 ℃; for 1.5h;

DOI:10.1002/chem.200400407

Reference yield:

(-)-(4aS,8aS)-3,4,4a,5,6,7,8,8a-octahydro-5,5,8a-trimethylnaphthalen-1(2H)-one (60134-39-6) → methyl 4-[(1S,2S)-2-hydroxy-2,6,6-trimethylcyclohexyl]butanoate (680218-11-5)

Guidance literature:

Multi-step reaction with 3 steps

1: 93 percent / m-chloroperoxybenzoic acid; NaHCO₃ / CH₂Cl₂ / 1.5 h / 20 °C

2: sodium hydroxide / ethanol; H₂O / 2.3 h / 20 °C

3: 97 mg / diethyl ether / 0 °C

With sodium hydroxide; sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid; In diethyl ether; ethanol; dichloromethane; water; 1: Baeyer-Villiger reaction;

DOI:10.1081/SCC-120027252

Reference yield:

(1S,7S)-1,8,8-trimethyl-2-oxabicyclo[5.4.0]undecan-3-one (217467-50-0) → methyl 4-[(1S,2S)-2-hydroxy-2,6,6-trimethylcyclohexyl]butanoate (680218-11-5)

Guidance literature:

Multi-step reaction with 2 steps

1: sodium hydroxide / ethanol; H₂O / 2.3 h / 20 °C

2: 97 mg / diethyl ether / 0 °C

With sodium hydroxide; In diethyl ether; ethanol; water;

DOI:10.1081/SCC-120027252

upstream raw materials:

diazomethane

methanol

(1S,7S)-1,8,8-trimethyl-2-oxabicyclo[5.4.0]undecan-3-one

(-)-(4aS,8aS)-3,4,4a,5,6,7,8,8a-octahydro-5,5,8a-trimethylnaphthalen-1(2H)-one

Downstream raw materials:

2-[2-((1S,2S)-2-hydroxy-2,6,6-trimethylcyclohexyl)ethyl]-3-hydroxybutyl 4-methylbenzenesulfonate

2-[2-((1S,2S)-2-hydroxy-2,6,6-trimethylcyclohexyl)ethyl]-3-oxobutyl 4-methylbenzenesulfonate

3-[2-((2S)-2-hydroxy-2,6,6-trimethylcyclohexyl)ethyl]but-3-en-2-one

2-[2-((1S,2S)-2-hydroxy-2,6,6-trimethylcyclohexyl)ethyl]butane-1,3-diol