[(1R,2S)-2-Hydroxy-1-((S)-1-hydroxy-ethyl)-pent-4-enyl]-carbamic acid benzyl ester

Base Information

Chemical Name:[(1R,2S)-2-Hydroxy-1-((S)-1-hydroxy-ethyl)-pent-4-enyl]-carbamic acid benzyl ester
CAS No.:201158-42-1
Molecular Formula:C₁₅H₂₁NO₄
Molecular Weight:279.336
Hs Code.:

Synonyms:[(1R,2S)-2-Hydroxy-1-((S)-1-hydroxy-ethyl)-pent-4-enyl]-carbamic acid benzyl ester

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Chemical Property of [(1R,2S)-2-Hydroxy-1-((S)-1-hydroxy-ethyl)-pent-4-enyl]-carbamic acid benzyl ester

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Technology Process of [(1R,2S)-2-Hydroxy-1-((S)-1-hydroxy-ethyl)-pent-4-enyl]-carbamic acid benzyl ester

There total 5 articles about [(1R,2S)-2-Hydroxy-1-((S)-1-hydroxy-ethyl)-pent-4-enyl]-carbamic acid benzyl 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: 78.0%

: 201158-37-4
(2S,3R)-3-benzyloxycarbonylamino-2-hydroxyhept-6-en-4-one

: 201158-42-1
[(1R,2S)-2-Hydroxy-1-((S)-1-hydroxy-ethyl)-pent-4-enyl]-carbamic acid benzyl ester

Guidance literature:: With tetramethylammonium triacetoxyborohydride; In acetic acid; acetonitrile; at -28 ℃; for 4h;
DOI:10.1021/jo971380i

Reference yield:

: 5618-95-1,19728-63-3,41151-16-0,85995-53-5,119221-16-8,80384-27-6
(2R,3S)-2-{[(benzyloxy)carbonyl]amino}-3-hydroxybutanoic acid

: 201158-42-1
[(1R,2S)-2-Hydroxy-1-((S)-1-hydroxy-ethyl)-pent-4-enyl]-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 73 percent / p-toluenesulfonic acid / benzene / 3 h / Heating

2: 72 percent / cyanuric chloride, pyridine / CH₂Cl₂ / 50 h

3: 86 percent / tetrahydrofuran; diethyl ether / 2.5 h / -78 °C

4: 64 percent / TFA / methanol / 0.25 h

5: 78 percent / tetramethylammonium triacetoxyborohydride / acetic acid; acetonitrile / 4 h / -28 °C

With pyridine; 1,3,5-trichloro-2,4,6-triazine; toluene-4-sulfonic acid; trifluoroacetic acid; tetramethylammonium triacetoxyborohydride; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; acetic acid; acetonitrile; benzene;
DOI:10.1021/jo971380i

Reference yield:

: (4S,5S)-4-But-3-enoyl-2,2,5-trimethyl-oxazolidine-3-carboxylic acid benzyl ester

: 201158-42-1
[(1R,2S)-2-Hydroxy-1-((S)-1-hydroxy-ethyl)-pent-4-enyl]-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 64 percent / TFA / methanol / 0.25 h

2: 78 percent / tetramethylammonium triacetoxyborohydride / acetic acid; acetonitrile / 4 h / -28 °C

With trifluoroacetic acid; tetramethylammonium triacetoxyborohydride; In methanol; acetic acid; acetonitrile;
DOI:10.1021/jo971380i