(S)-2--4-pentenoic Acid

Base Information

Chemical Name:(S)-2--4-pentenoic Acid
CAS No.:109468-24-8
Molecular Formula:C₂₀H₂₁NO₄
Molecular Weight:339.391
Hs Code.:

(S)-2-<N-Benzyl-N-(benzyloxycarbonyl)amino>-4-pentenoic Acid

Synonyms:

Suppliers and Price of (S)-2--4-pentenoic Acid

Supply Marketing:

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

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Chemical Property of (S)-2--4-pentenoic Acid

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of (S)-2--4-pentenoic Acid

There total 6 articles about (S)-2--4-pentenoic Acid 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:

: 917-57-7
vinyllithium

: 109468-08-8
Benzyl-((S)-2-oxo-oxetan-3-yl)-carbamic acid benzyl ester

: 109468-24-8
(S)-2--4-pentenoic Acid

Guidance literature:: With 1.) CuCN; Yield given. Multistep reaction; 1.) THF, 2.) -78 deg C, 1 h, -46 deg C, 3 h, 0 deg C, 30 min;
DOI:10.1021/ja00249a031

Reference yield:

: (S)-2-(Benzyl-benzyloxycarbonyl-amino)-pent-4-enoic acid methyl ester

: 109468-24-8
(S)-2--4-pentenoic Acid

Guidance literature:: With sodium hydroxide; In methanol; for 3h;
DOI:10.1021/jo0485738

Reference yield:

: 16338-48-0
L-allylglycine

: 109468-24-8
(S)-2--4-pentenoic Acid

Guidance literature:: Multi-step reaction with 5 steps

1: SOCl₂ / 50 °C

2: Et₃N / methanol / 3 h

3: 1.58 g / NaBH₄ / methanol / 0.5 h / 0 °C

4: aq. Na₂CO₃ / ethyl acetate / 18 h / 20 °C

5: 0.82 g / aq. NaOH / methanol / 3 h

With sodium hydroxide; sodium tetrahydroborate; thionyl chloride; sodium carbonate; triethylamine; In methanol; ethyl acetate;
DOI:10.1021/jo0485738