2-Benzyloxy-1-((3aR,5S,6S,6aR)-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanone

Base Information

Chemical Name:2-Benzyloxy-1-((3aR,5S,6S,6aR)-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanone
CAS No.:114144-68-2
Molecular Formula:C₁₇H₂₂O₅
Molecular Weight:306.359
Hs Code.:

Synonyms:2-Benzyloxy-1-((3aR,5S,6S,6aR)-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanone

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Chemical Property of 2-Benzyloxy-1-((3aR,5S,6S,6aR)-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanone

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Technology Process of 2-Benzyloxy-1-((3aR,5S,6S,6aR)-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanone

There total 4 articles about 2-Benzyloxy-1-((3aR,5S,6S,6aR)-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanone 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: 89.0%

: 114144-67-1
6-O-benzyl-3-deoxy-1,2-O-isopropylidene-3-C-methyl-α-D-allofuranose

: 114144-68-2
2-Benzyloxy-1-((3aR,5S,6S,6aR)-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanone

Guidance literature:: With 3 A molecular sieve; pyridinium chlorochromate; In dichloromethane; for 24h; Ambient temperature;
DOI:10.1248/cpb.35.2184

Reference yield:

: 26291-75-8,81114-49-0,109200-09-1,128461-80-3
(R)-1-((3aR,5S,6R,6aR)-2,2,6-trimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl)ethane-1,2-diol

: 114144-68-2
2-Benzyloxy-1-((3aR,5S,6S,6aR)-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanone

Guidance literature:: Multi-step reaction with 2 steps

1.1: di-n-butyltin oxide / toluene / 3 h / Heating

1.2: 66 percent / cesium fluoride / dimethylformamide / 18 h / 20 °C

2.1: CrO₃; aq. sulfuric acid / acetone / 1 h / 0 °C

With chromium(VI) oxide; sulfuric acid; di(n-butyl)tin oxide; In acetone; toluene; 1.1: stannylation / 1.2: Alkylation / 2.1: Jones oxidation;
DOI:10.1016/S0040-4020(97)01015-6

Reference yield:

: 100-39-0
benzyl bromide

: 114144-68-2
2-Benzyloxy-1-((3aR,5S,6S,6aR)-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanone

Guidance literature:: Multi-step reaction with 2 steps

1.1: di-n-butyltin oxide / toluene / 3 h / Heating

1.2: 66 percent / cesium fluoride / dimethylformamide / 18 h / 20 °C

2.1: CrO₃; aq. sulfuric acid / acetone / 1 h / 0 °C

With chromium(VI) oxide; sulfuric acid; di(n-butyl)tin oxide; In acetone; toluene; 1.1: stannylation / 1.2: Alkylation / 2.1: Jones oxidation;
DOI:10.1016/S0040-4020(97)01015-6