2-(benzyloxycarbonylamino)-2-methylpropyl 3-(acetylthio)-2,2-dimethylpropanoate

Base Information

Chemical Name:2-(benzyloxycarbonylamino)-2-methylpropyl 3-(acetylthio)-2,2-dimethylpropanoate
CAS No.:1037832-92-0
Molecular Formula:C₁₉H₂₇NO₅S
Molecular Weight:381.493
Hs Code.:

Synonyms:2-(benzyloxycarbonylamino)-2-methylpropyl 3-(acetylthio)-2,2-dimethylpropanoate

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Chemical Property of 2-(benzyloxycarbonylamino)-2-methylpropyl 3-(acetylthio)-2,2-dimethylpropanoate

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Technology Process of 2-(benzyloxycarbonylamino)-2-methylpropyl 3-(acetylthio)-2,2-dimethylpropanoate

There total 3 articles about 2-(benzyloxycarbonylamino)-2-methylpropyl 3-(acetylthio)-2,2-dimethylpropanoate 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: 71.0%

: 1037832-91-9
2-(benzyloxycarbonylamino)-2-methylpropyl 3-chloro-2,2-dimethylpropanoate

: 10387-40-3
potassium thioacetate

: 1037832-92-0
2-(benzyloxycarbonylamino)-2-methylpropyl 3-(acetylthio)-2,2-dimethylpropanoate

Guidance literature:: In N,N-dimethyl-formamide; at 100 ℃; for 5h;

Reference yield:

: 4300-97-4
3-Chloropivaloyl chloride

: 1037832-92-0
2-(benzyloxycarbonylamino)-2-methylpropyl 3-(acetylthio)-2,2-dimethylpropanoate

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane / 48 h / 0 - 20 °C

2: N,N-dimethyl-formamide / 5 h / 100 °C

With N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 62471-40-3
2-benzyloxycarbonylamino-2-methylpropanol

: 1037832-92-0
2-(benzyloxycarbonylamino)-2-methylpropyl 3-(acetylthio)-2,2-dimethylpropanoate

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane / 48 h / 0 - 20 °C

2: N,N-dimethyl-formamide / 5 h / 100 °C

With N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide;