(R)-3-benzyl-4-((1R,2R,Z)-2-(benzyloxy)-1-hydroxyhexadec-3-enyl)oxazolidin-2-one

Base Information

Chemical Name:(R)-3-benzyl-4-((1R,2R,Z)-2-(benzyloxy)-1-hydroxyhexadec-3-enyl)oxazolidin-2-one
CAS No.:1383970-67-9
Molecular Formula:C₃₃H₄₇NO₄
Molecular Weight:521.74
Hs Code.:

Synonyms:(R)-3-benzyl-4-((1R,2R,Z)-2-(benzyloxy)-1-hydroxyhexadec-3-enyl)oxazolidin-2-one

Suppliers and Price of (R)-3-benzyl-4-((1R,2R,Z)-2-(benzyloxy)-1-hydroxyhexadec-3-enyl)oxazolidin-2-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (R)-3-benzyl-4-((1R,2R,Z)-2-(benzyloxy)-1-hydroxyhexadec-3-enyl)oxazolidin-2-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R)-3-benzyl-4-((1R,2R,Z)-2-(benzyloxy)-1-hydroxyhexadec-3-enyl)oxazolidin-2-one

There total 7 articles about (R)-3-benzyl-4-((1R,2R,Z)-2-(benzyloxy)-1-hydroxyhexadec-3-enyl)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:

: C₂₀H₂₁NO₅

: 13266-02-9
n-tridecyltriphenylphosphonium bromide

: 1383970-67-9
(R)-3-benzyl-4-((1R,2R,Z)-2-(benzyloxy)-1-hydroxyhexadec-3-enyl)oxazolidin-2-one

Guidance literature:: n-tridecyltriphenylphosphonium bromide; With n-butyllithium; In tetrahydrofuran; hexane; at 0 ℃; for 0.5h; Inert atmosphere;

C₂₀H₂₁NO₅; In tetrahydrofuran; hexane; at 0 ℃; for 0.5h; Inert atmosphere;
DOI:10.1016/j.tetasy.2012.04.009

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

: 1383970-67-9
(R)-3-benzyl-4-((1R,2R,Z)-2-(benzyloxy)-1-hydroxyhexadec-3-enyl)oxazolidin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium tetrahydroborate / methanol / 2 h / 0 °C

1.2: Saturated solution

2.1: sodium hydride / tetrahydrofuran; mineral oil / 20 °C / Cooling with ice

3.1: trifluoroacetic acid / water / 3 h / 0 - 20 °C

4.1: sodium periodate; sodium hydrogencarbonate / methanol; water / 2 h / 0 °C

5.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / 0 °C / Inert atmosphere

5.2: 0.5 h / 0 °C / Inert atmosphere

With sodium tetrahydroborate; sodium periodate; n-butyllithium; sodium hydride; sodium hydrogencarbonate; trifluoroacetic acid; In tetrahydrofuran; methanol; hexane; water; mineral oil; 5.1: Wittig reaction / 5.2: Wittig reaction;
DOI:10.1016/j.tetasy.2012.04.009

Reference yield:

: 1383970-64-6
benzyl benzyl((R)-1-((3aR,5R,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-2-hydroxyethyl)carbamate

: 1383970-67-9
(R)-3-benzyl-4-((1R,2R,Z)-2-(benzyloxy)-1-hydroxyhexadec-3-enyl)oxazolidin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / tetrahydrofuran; mineral oil / 20 °C / Cooling with ice

2.1: trifluoroacetic acid / water / 3 h / 0 - 20 °C

3.1: sodium periodate; sodium hydrogencarbonate / methanol; water / 2 h / 0 °C

4.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / 0 °C / Inert atmosphere

4.2: 0.5 h / 0 °C / Inert atmosphere

With sodium periodate; n-butyllithium; sodium hydride; sodium hydrogencarbonate; trifluoroacetic acid; In tetrahydrofuran; methanol; hexane; water; mineral oil; 4.1: Wittig reaction / 4.2: Wittig reaction;
DOI:10.1016/j.tetasy.2012.04.009