Acetic acid (1R,2R,3S,4S,5S)-3-benzyloxymethyl-4-(2-methoxy-ethoxymethoxy)-6-oxa-bicyclo[3.1.0]hex-2-yl ester

Base Information

Chemical Name:Acetic acid (1R,2R,3S,4S,5S)-3-benzyloxymethyl-4-(2-methoxy-ethoxymethoxy)-6-oxa-bicyclo[3.1.0]hex-2-yl ester
CAS No.:143994-97-2
Molecular Formula:C₁₉H₂₆O₇
Molecular Weight:366.411
Hs Code.:

Synonyms:Acetic acid (1R,2R,3S,4S,5S)-3-benzyloxymethyl-4-(2-methoxy-ethoxymethoxy)-6-oxa-bicyclo[3.1.0]hex-2-yl ester

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Chemical Property of Acetic acid (1R,2R,3S,4S,5S)-3-benzyloxymethyl-4-(2-methoxy-ethoxymethoxy)-6-oxa-bicyclo[3.1.0]hex-2-yl ester

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Technology Process of Acetic acid (1R,2R,3S,4S,5S)-3-benzyloxymethyl-4-(2-methoxy-ethoxymethoxy)-6-oxa-bicyclo[3.1.0]hex-2-yl ester

There total 4 articles about Acetic acid (1R,2R,3S,4S,5S)-3-benzyloxymethyl-4-(2-methoxy-ethoxymethoxy)-6-oxa-bicyclo[3.1.0]hex-2-yl 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: 81.0%

: 3970-21-6
2-Methoxyethoxymethyl chloride

: 143994-96-1
Acetic acid (1R,2R,3S,4S,5S)-3-benzyloxymethyl-4-hydroxy-6-oxa-bicyclo[3.1.0]hex-2-yl ester

: 143994-97-2
Acetic acid (1R,2R,3S,4S,5S)-3-benzyloxymethyl-4-(2-methoxy-ethoxymethoxy)-6-oxa-bicyclo[3.1.0]hex-2-yl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; for 48h;

Reference yield:

: 144069-03-4
(+)-(1α,2β,3α)-1-acetoxy-2-<(phenylmethoxy)methyl>cyclopent-4-en-3-ol

: 143994-97-2
Acetic acid (1R,2R,3S,4S,5S)-3-benzyloxymethyl-4-(2-methoxy-ethoxymethoxy)-6-oxa-bicyclo[3.1.0]hex-2-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / m-chloroperoxybenzoic acid / CH₂Cl₂ / 24 h / 0 deg C to r.t.

2: 81 percent / i-Pr₂NEt / CH₂Cl₂ / 48 h

With N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; In dichloromethane;

Reference yield:

: 134756-61-9
(1α,2β,3α)-2-<(benzyloxy)methyl>-4-cyclopentene-1,3-diol diacetate

: 143994-97-2
Acetic acid (1R,2R,3S,4S,5S)-3-benzyloxymethyl-4-(2-methoxy-ethoxymethoxy)-6-oxa-bicyclo[3.1.0]hex-2-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / 168 h / Ambient temperature; porcine pancreatic lipase, phosphate buffer, pH 7

2: 1.) m-chloroperoxybenzoic acid, 2.) i-Pr₂NEt / 1.) CH₂Cl₂, 0 deg C to r.t., 24 h, 2.) CH₂Cl₂, r.t., 48 h

With N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid;