(1aS,2R,3R,3aS,6aR,6bS)-2-Cyclohexylmethyl-5,5-dimethyl-hexahydro-1,4,6-trioxa-cyclopropa[e]inden-3-ol

Base Information

Chemical Name:(1aS,2R,3R,3aS,6aR,6bS)-2-Cyclohexylmethyl-5,5-dimethyl-hexahydro-1,4,6-trioxa-cyclopropa[e]inden-3-ol
CAS No.:180165-11-1
Molecular Formula:C₁₆H₂₆O₄
Molecular Weight:282.38
Hs Code.:

Synonyms:(1aS,2R,3R,3aS,6aR,6bS)-2-Cyclohexylmethyl-5,5-dimethyl-hexahydro-1,4,6-trioxa-cyclopropa[e]inden-3-ol

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Chemical Property of (1aS,2R,3R,3aS,6aR,6bS)-2-Cyclohexylmethyl-5,5-dimethyl-hexahydro-1,4,6-trioxa-cyclopropa[e]inden-3-ol

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Technology Process of (1aS,2R,3R,3aS,6aR,6bS)-2-Cyclohexylmethyl-5,5-dimethyl-hexahydro-1,4,6-trioxa-cyclopropa[e]inden-3-ol

There total 4 articles about (1aS,2R,3R,3aS,6aR,6bS)-2-Cyclohexylmethyl-5,5-dimethyl-hexahydro-1,4,6-trioxa-cyclopropa[e]inden-3-ol 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: 78.0%

: 180322-50-3
(3aS,4R,5S,7aR)-5-Cyclohexylmethyl-2,2-dimethyl-3a,4,5,7a-tetrahydro-benzo[1,3]dioxol-4-ol

: 180165-11-1
(1aS,2R,3R,3aS,6aR,6bS)-2-Cyclohexylmethyl-5,5-dimethyl-hexahydro-1,4,6-trioxa-cyclopropa[e]inden-3-ol

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; for 48h; Ambient temperature;
DOI:10.1055/s-1996-4440

Reference yield:

: 35166-78-0
cyclohexylmethyl magnesium bromide

: 180165-11-1
(1aS,2R,3R,3aS,6aR,6bS)-2-Cyclohexylmethyl-5,5-dimethyl-hexahydro-1,4,6-trioxa-cyclopropa[e]inden-3-ol

Guidance literature:: Multi-step reaction with 3 steps

1: 38 percent / CuI / tetrahydrofuran / 10 h / -78 - 0 °C

2: 80 percent / NaOEt / ethanol / 2 h / Heating

3: 78 percent / meta-chloroperoxybenzoic acid / CH₂Cl₂ / 48 h / Ambient temperature

With copper(l) iodide; sodium ethanolate; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1055/s-1996-4440

Reference yield:

: 138913-30-1
(1R,4S,5S,6R)-3-chloro-4,5-O-isopropylidene-7-oxabicyclo[4.1.0]hept-2-ene-4,5-diol

: 180165-11-1
(1aS,2R,3R,3aS,6aR,6bS)-2-Cyclohexylmethyl-5,5-dimethyl-hexahydro-1,4,6-trioxa-cyclopropa[e]inden-3-ol

Guidance literature:: Multi-step reaction with 3 steps

1: 38 percent / CuI / tetrahydrofuran / 10 h / -78 - 0 °C

2: 80 percent / NaOEt / ethanol / 2 h / Heating

3: 78 percent / meta-chloroperoxybenzoic acid / CH₂Cl₂ / 48 h / Ambient temperature

With copper(l) iodide; sodium ethanolate; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1055/s-1996-4440