3-benzyl-4-((2R,1S,5S)-2-isopropyl-5-methylcyclohexyloxy)-4-oxobutanoic acid

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Chemical Name:3-benzyl-4-((2R,1S,5S)-2-isopropyl-5-methylcyclohexyloxy)-4-oxobutanoic acid
CAS No.:1415314-31-6
Molecular Formula:C₂₁H₃₀O₄
Molecular Weight:346.467
Hs Code.:

Synonyms:3-benzyl-4-((2R,1S,5S)-2-isopropyl-5-methylcyclohexyloxy)-4-oxobutanoic acid

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Chemical Property of 3-benzyl-4-((2R,1S,5S)-2-isopropyl-5-methylcyclohexyloxy)-4-oxobutanoic acid

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Technology Process of 3-benzyl-4-((2R,1S,5S)-2-isopropyl-5-methylcyclohexyloxy)-4-oxobutanoic acid

There total 2 articles about 3-benzyl-4-((2R,1S,5S)-2-isopropyl-5-methylcyclohexyloxy)-4-oxobutanoic acid 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: 64.0%

: 204326-53-4
4-((2R,1S,5S)-2-isopropyl-5-methylcyclohexyloxy)-4-oxobutanoic acid

: 1415314-31-6
3-benzyl-4-((2R,1S,5S)-2-isopropyl-5-methylcyclohexyloxy)-4-oxobutanoic acid

Guidance literature:: 4-((2R,1S,5S)-2-isopropyl-5-methylcyclohexyloxy)-4-oxobutanoic acid; With n-butyllithium; diisopropylamine; In tetrahydrofuran; at -78 - -20 ℃; Inert atmosphere;

benzyl halide; In tetrahydrofuran; at -20 - 20 ℃; Inert atmosphere;
DOI:10.2174/157017812803521072

Reference yield:

: 15356-60-2
(1S,2R,5S)-(+)-menthol

: 1415314-31-6
3-benzyl-4-((2R,1S,5S)-2-isopropyl-5-methylcyclohexyloxy)-4-oxobutanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: sulfuric acid / chloroform / 0.5 h / Reflux

2.1: n-butyllithium; diisopropylamine / tetrahydrofuran / -78 - -20 °C / Inert atmosphere

2.2: -20 - 20 °C / Inert atmosphere

With n-butyllithium; sulfuric acid; diisopropylamine; In tetrahydrofuran; chloroform;
DOI:10.2174/157017812803521072