Allyl-[(R)-2-((R)-4-benzyl-2-oxo-oxazolidine-3-carbonyl)-pent-4-enyl]-carbamic acid tert-butyl ester

Base Information

Chemical Name:Allyl-[(R)-2-((R)-4-benzyl-2-oxo-oxazolidine-3-carbonyl)-pent-4-enyl]-carbamic acid tert-butyl ester
CAS No.:851593-74-3
Molecular Formula:C₂₄H₃₂N₂O₅
Molecular Weight:428.528
Hs Code.:

Synonyms:Allyl-[(R)-2-((R)-4-benzyl-2-oxo-oxazolidine-3-carbonyl)-pent-4-enyl]-carbamic acid tert-butyl ester

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Chemical Property of Allyl-[(R)-2-((R)-4-benzyl-2-oxo-oxazolidine-3-carbonyl)-pent-4-enyl]-carbamic acid tert-butyl ester

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Technology Process of Allyl-[(R)-2-((R)-4-benzyl-2-oxo-oxazolidine-3-carbonyl)-pent-4-enyl]-carbamic acid tert-butyl ester

There total 5 articles about Allyl-[(R)-2-((R)-4-benzyl-2-oxo-oxazolidine-3-carbonyl)-pent-4-enyl]-carbamic acid tert-butyl ester 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: 64.0%

: 851593-73-2
allyl-[3-(4-benzyl-2-oxo-oxazolidin-3-yl)-3-oxo-propyl]-carbamic acid tert-butyl ester

: 556-56-9
allyl iodid

: 851593-74-3
Allyl-[(R)-2-((R)-4-benzyl-2-oxo-oxazolidine-3-carbonyl)-pent-4-enyl]-carbamic acid tert-butyl ester

: Allyl-[(S)-2-((R)-4-benzyl-2-oxo-oxazolidine-3-carbonyl)-pent-4-enyl]-carbamic acid tert-butyl ester

Guidance literature:: allyl-[3-(4-benzyl-2-oxo-oxazolidin-3-yl)-3-oxo-propyl]-carbamic acid tert-butyl ester; With sodium hexamethyldisilazane; In tetrahydrofuran; at -78 ℃;

allyl iodid; In tetrahydrofuran; at -78 - 0 ℃;
DOI:10.1055/s-2005-863719

Reference yield:

: 355390-94-2
3-(allyl-tert-butoxycarbonyl-amino)-propionic acid

: 851593-74-3
Allyl-[(R)-2-((R)-4-benzyl-2-oxo-oxazolidine-3-carbonyl)-pent-4-enyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: Et₃N / tetrahydrofuran

2.1: n-BuLi

3.1: NaN(TMS)2 / tetrahydrofuran / -78 °C

3.2: 64 percent / tetrahydrofuran / -78 - 0 °C

With n-butyllithium; sodium hexamethyldisilazane; triethylamine; In tetrahydrofuran;
DOI:10.1055/s-2005-863719

Reference yield:

: C₁₆H₂₇NO₅

: 851593-74-3
Allyl-[(R)-2-((R)-4-benzyl-2-oxo-oxazolidine-3-carbonyl)-pent-4-enyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-BuLi

2.1: NaN(TMS)2 / tetrahydrofuran / -78 °C

2.2: 64 percent / tetrahydrofuran / -78 - 0 °C

With n-butyllithium; sodium hexamethyldisilazane; In tetrahydrofuran;
DOI:10.1055/s-2005-863719