(4R)-3-[1-oxo-2-[(R)-1-(benzyloxymethyl)but-3-enyl-1-oxy]-ethyl]-4-benzyl-1,3-oxazolidinone

Base Information

Chemical Name:(4R)-3-[1-oxo-2-[(R)-1-(benzyloxymethyl)but-3-enyl-1-oxy]-ethyl]-4-benzyl-1,3-oxazolidinone
CAS No.:284471-60-9
Molecular Formula:C₂₄H₂₇NO₅
Molecular Weight:409.482
Hs Code.:

Synonyms:(4R)-3-[1-oxo-2-[(R)-1-(benzyloxymethyl)but-3-enyl-1-oxy]-ethyl]-4-benzyl-1,3-oxazolidinone

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Chemical Property of (4R)-3-[1-oxo-2-[(R)-1-(benzyloxymethyl)but-3-enyl-1-oxy]-ethyl]-4-benzyl-1,3-oxazolidinone

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Technology Process of (4R)-3-[1-oxo-2-[(R)-1-(benzyloxymethyl)but-3-enyl-1-oxy]-ethyl]-4-benzyl-1,3-oxazolidinone

There total 3 articles about (4R)-3-[1-oxo-2-[(R)-1-(benzyloxymethyl)but-3-enyl-1-oxy]-ethyl]-4-benzyl-1,3-oxazolidinone 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:

: 40217-17-2,90719-32-7,120574-96-1,102029-44-7
(R)-4-(phenylmethyl)-2-oxazolidinone

: C₁₉H₂₆O₅

: 284471-60-9
(4R)-3-[1-oxo-2-[(R)-1-(benzyloxymethyl)but-3-enyl-1-oxy]-ethyl]-4-benzyl-1,3-oxazolidinone

Guidance literature:: (R)-4-(phenylmethyl)-2-oxazolidinone; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.166667h;

C₁₉H₂₆O₅; In tetrahydrofuran; diethyl ether; hexane; at -78 - 0 ℃; Further stages.;
DOI:10.1021/ja0007197

Reference yield:

: 58931-16-1,88981-35-5,110339-28-1
(R)-1-benzyloxypent-4-en-2-ol

: 284471-60-9
(4R)-3-[1-oxo-2-[(R)-1-(benzyloxymethyl)but-3-enyl-1-oxy]-ethyl]-4-benzyl-1,3-oxazolidinone

Guidance literature:: Multi-step reaction with 3 steps

1.1: 93 percent / NaH / tetrahydrofuran / 14 h / 25 °C

2.1: Et₃N / diethyl ether / 1 h / 0 °C

3.1: nBuLi / tetrahydrofuran; hexane / 0.17 h / -78 °C

3.2: 15.3 g / tetrahydrofuran; diethyl ether; hexane / -78 - 0 °C

With n-butyllithium; sodium hydride; triethylamine; In tetrahydrofuran; diethyl ether; hexane; 1.1: Alkylation / 2.1: Acylation / 3.1: Metallation / 3.2: Acylation;
DOI:10.1021/ja0007197

Reference yield:

: 239075-68-4
(R)-1-(benzyloxymethyl)but-3-enyl-1-oxyacetic acid

: 284471-60-9
(4R)-3-[1-oxo-2-[(R)-1-(benzyloxymethyl)but-3-enyl-1-oxy]-ethyl]-4-benzyl-1,3-oxazolidinone

Guidance literature:: Multi-step reaction with 2 steps

1.1: Et₃N / diethyl ether / 1 h / 0 °C

2.1: nBuLi / tetrahydrofuran; hexane / 0.17 h / -78 °C

2.2: 15.3 g / tetrahydrofuran; diethyl ether; hexane / -78 - 0 °C

With n-butyllithium; triethylamine; In tetrahydrofuran; diethyl ether; hexane; 1.1: Acylation / 2.1: Metallation / 2.2: Acylation;
DOI:10.1021/ja0007197