[(1S,2R)-2-Hydroxy-1-isobutyl-3-(4-methoxy-benzyloxymethyl)-but-3-enyl]-carbamic acid benzyl ester

Base Information

• Chemical Name: [(1S,2R)-2-Hydroxy-1-isobutyl-3-(4-methoxy-benzyloxymethyl)-but-3-enyl]-carbamic acid benzyl ester
• CAS No.: 147298-38-2
• Molecular Formula: C₂₅H₃₃NO₅
• Molecular Weight: 427.541

Synonyms:[(1S,2R)-2-Hydroxy-1-isobutyl-3-(4-methoxy-benzyloxymethyl)-but-3-enyl]-carbamic acid benzyl ester

Chemical Property of [(1S,2R)-2-Hydroxy-1-isobutyl-3-(4-methoxy-benzyloxymethyl)-but-3-enyl]-carbamic acid benzyl ester

Chemical Property:

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Technology Process of [(1S,2R)-2-Hydroxy-1-isobutyl-3-(4-methoxy-benzyloxymethyl)-but-3-enyl]-carbamic acid benzyl ester

There total 3 articles about [(1S,2R)-2-Hydroxy-1-isobutyl-3-(4-methoxy-benzyloxymethyl)-but-3-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: 22.0%

(R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1R,2S)-2-benzyloxycarbonylamino-1-[1-(4-methoxy-benzyloxymethyl)-vinyl]-4-methyl-pentyl ester (147298-43-9) → [(1S,2R)-2-Hydroxy-1-isobutyl-3-(4-methoxy-benzyloxymethyl)-but-3-enyl]-carbamic acid benzyl ester (147298-38-2) + (4S,5R)-4-Isobutyl-5-[1-(4-methoxy-benzyloxymethyl)-vinyl]-oxazolidin-2-one

Guidance literature:

With sodium methylate; In methanol; for 4h; Ambient temperature;

DOI:10.1016/S0040-4039(00)77488-0

Reference yield:

1-(((2-bromoallyl)oxy)methyl)-4-methoxybenzene (147298-36-0) → [(1S,2R)-2-Hydroxy-1-isobutyl-3-(4-methoxy-benzyloxymethyl)-but-3-enyl]-carbamic acid benzyl ester (147298-38-2)

Guidance literature:

Multi-step reaction with 2 steps

2: 50 percent / NaOMe / methanol / 4 h / Ambient temperature

With sodium methylate; In methanol;

DOI:10.1016/S0040-4039(00)77488-0

Reference yield:

p-methoxybenzyl chloride (824-94-2) → [(1S,2R)-2-Hydroxy-1-isobutyl-3-(4-methoxy-benzyloxymethyl)-but-3-enyl]-carbamic acid benzyl ester (147298-38-2)

Guidance literature:

Multi-step reaction with 3 steps

1: 1) n-BuLi

3: 50 percent / NaOMe / methanol / 4 h / Ambient temperature

With n-butyllithium; sodium methylate; In methanol;

DOI:10.1016/S0040-4039(00)77488-0

upstream raw materials:

(R)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1R,2S)-2-benzyloxycarbonylamino-1-[1-(4-methoxy-benzyloxymethyl)-vinyl]-4-methyl-pentyl ester

1-(((2-bromoallyl)oxy)methyl)-4-methoxybenzene

p-methoxybenzyl chloride

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