(4R,5R)-3-Benzyl-4-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-5-vinyl-oxazolidin-2-one

Base Information

Chemical Name:(4R,5R)-3-Benzyl-4-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-5-vinyl-oxazolidin-2-one
CAS No.:899431-71-1
Molecular Formula:C₂₆H₂₉NO₆
Molecular Weight:451.519
Hs Code.:

Synonyms:(4R,5R)-3-Benzyl-4-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-5-vinyl-oxazolidin-2-one

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Chemical Property of (4R,5R)-3-Benzyl-4-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-5-vinyl-oxazolidin-2-one

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Technology Process of (4R,5R)-3-Benzyl-4-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-5-vinyl-oxazolidin-2-one

There total 6 articles about (4R,5R)-3-Benzyl-4-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-5-vinyl-oxazolidin-2-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:

: Benzyl-[(S)-1-((2R,3R,4R,5S)-3-benzyloxy-4,5-dihydroxy-tetrahydro-furan-2-yl)-2-oxo-ethyl]-carbamic acid benzyl ester

: 899431-71-1
(4R,5R)-3-Benzyl-4-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-5-vinyl-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 2.90 g / sodium metaperiodate / acetone; H₂O / 6 h

2: tetrahydrofuran / 1 h / -50 °C

3: 1.2 g / aq. KOH / methanol / 0.17 h / 90 °C

With potassium hydroxide; sodium periodate; In tetrahydrofuran; methanol; water; acetone; 2: Grignard reaction;
DOI:10.1021/jo0601617

Reference yield:

: 899431-70-0
Benzyl-[(S)-1-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-2-oxo-ethyl]-carbamic acid benzyl ester

: 899431-71-1
(4R,5R)-3-Benzyl-4-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-5-vinyl-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: tetrahydrofuran / 1 h / -50 °C

2: 1.2 g / aq. KOH / methanol / 0.17 h / 90 °C

With potassium hydroxide; In tetrahydrofuran; methanol; 1: Grignard reaction;
DOI:10.1021/jo0601617

Reference yield:

: 899431-69-7
3-O-benzyl-1,2-O-isopropylidene-5,6,7-trideoxy-5-(N-benzyl-N-benzoxycarbonylamino)-α-D-gluco-6-eno-hepta-1,4-furanose

: 899431-71-1
(4R,5R)-3-Benzyl-4-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-5-vinyl-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: NMO; potassium osmate / acetone; H₂O / 12 h / 20 °C

2: 2.90 g / sodium metaperiodate / acetone; H₂O / 6 h

3: tetrahydrofuran / 1 h / -50 °C

4: 1.2 g / aq. KOH / methanol / 0.17 h / 90 °C

With potassium hydroxide; potassium osmate(VI); sodium periodate; N-methyl-2-indolinone; In tetrahydrofuran; methanol; water; acetone; 3: Grignard reaction;
DOI:10.1021/jo0601617