(1R,2R,4S,6S)-2-(benzyloxy)-4-methyl-3,7-dioxabicyclo[4.1.0]-heptan-5-one

Base Information

Chemical Name:(1R,2R,4S,6S)-2-(benzyloxy)-4-methyl-3,7-dioxabicyclo[4.1.0]-heptan-5-one
CAS No.:1174754-24-5
Molecular Formula:C₁₃H₁₄O₄
Molecular Weight:234.252
Hs Code.:

Synonyms:(1R,2R,4S,6S)-2-(benzyloxy)-4-methyl-3,7-dioxabicyclo[4.1.0]-heptan-5-one

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Chemical Property of (1R,2R,4S,6S)-2-(benzyloxy)-4-methyl-3,7-dioxabicyclo[4.1.0]-heptan-5-one

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Technology Process of (1R,2R,4S,6S)-2-(benzyloxy)-4-methyl-3,7-dioxabicyclo[4.1.0]-heptan-5-one

There total 6 articles about (1R,2R,4S,6S)-2-(benzyloxy)-4-methyl-3,7-dioxabicyclo[4.1.0]-heptan-5-one 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: 90.0%

: 512809-21-1
benzyl 2,3,6-trideoxy-α-L-hex-2-enopyranosid-4-ulose

: 1174754-24-5
(1R,2R,4S,6S)-2-(benzyloxy)-4-methyl-3,7-dioxabicyclo[4.1.0]-heptan-5-one

Guidance literature:: With dihydrogen peroxide; sodium hydroxide; In methanol; water; at 20 ℃; for 6h; optical yield given as %de; diastereoselective reaction;
DOI:10.1039/c1cc13837e

Reference yield:

: 865484-73-7
tert-butyl ((2S,6S)-6-methyl-5-oxo-5,6-dihydro-2H-pyran-2-yl) carbonate

: 1174754-24-5
(1R,2R,4S,6S)-2-(benzyloxy)-4-methyl-3,7-dioxabicyclo[4.1.0]-heptan-5-one

Guidance literature:: Multi-step reaction with 2 steps

1: tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; triphenylphosphine / dichloromethane / 8 h / 0 °C

2: dihydrogen peroxide; sodium hydroxide / methanol; water / 6 h / 20 °C

With tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; dihydrogen peroxide; triphenylphosphine; sodium hydroxide; In methanol; dichloromethane; water;
DOI:10.1039/c1cc13837e

Reference yield:

: 1192-62-7,80145-44-4
1-(2-furyl)-1-ethanone

: 1174754-24-5
(1R,2R,4S,6S)-2-(benzyloxy)-4-methyl-3,7-dioxabicyclo[4.1.0]-heptan-5-one

Guidance literature:: Multi-step reaction with 5 steps

1: (R)-RuCl(η6-mesitylene)-(S,S)-TsDPEN; sodium formate; cetyltrimethylammonim bromide; sodium hydrogencarbonate / dichloromethane; water / 24 h / 20 °C

2: N-Bromosuccinimide; sodium acetate; sodium hydrogencarbonate / tetrahydrofuran; water / 1 h / 0 °C

3: dmap / dichloromethane / 12 h / -78 - -30 °C

4: tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; triphenylphosphine / dichloromethane / 8 h / 0 °C

5: dihydrogen peroxide; sodium hydroxide / methanol; water / 6 h / 20 °C

With dmap; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; N-Bromosuccinimide; (R)-RuCl(η6-mesitylene)-(S,S)-TsDPEN; dihydrogen peroxide; sodium formate; sodium acetate; cetyltrimethylammonim bromide; sodium hydrogencarbonate; triphenylphosphine; sodium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water;
DOI:10.1039/c1cc13837e