[(1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyl]-acetic acid tert-butyl ester

Base Information

Chemical Name:[(1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyl]-acetic acid tert-butyl ester
CAS No.:144599-66-6
Molecular Formula:C₂₀H₃₂NO₆P
Molecular Weight:413.451
Hs Code.:

Synonyms:[(1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyl]-acetic acid tert-butyl ester

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Chemical Property of [(1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyl]-acetic acid tert-butyl ester

Chemical Property:

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Technology Process of [(1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyl]-acetic acid tert-butyl ester

There total 11 articles about [(1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyl]-acetic 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:

: 90763-52-3,125882-52-2,125882-59-9,73270-45-8
diphenyl <1--3-methylbutyl>phosphonate

: 144599-66-6
[(1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyl]-acetic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 84 percent / MeONa / methanol / 22 °C

2: 87 percent / NaOH / methanol / 22 °C

3: SOCl₂ / CH₂Cl₂ / 22 °C

4: 56 percent / Et₃N / CH₂Cl₂ / 22 °C

5: tetrahydrofuran / 1.) -78 deg C; 2.) 0 deg C

With sodium hydroxide; thionyl chloride; sodium methylate; triethylamine; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/ja00327a046

Reference yield:

: 82629-28-5
dimethyl {1-[(benzyloxycarbonyl)amino]-3-methylbutyl}phosphonate

: 144599-66-6
[(1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyl]-acetic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 87 percent / NaOH / methanol / 22 °C

2: SOCl₂ / CH₂Cl₂ / 22 °C

3: 56 percent / Et₃N / CH₂Cl₂ / 22 °C

4: tetrahydrofuran / 1.) -78 deg C; 2.) 0 deg C

With sodium hydroxide; thionyl chloride; triethylamine; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/ja00327a046

Reference yield:

: 90763-54-5
methyl <1--3-methylbutyl>phosphonate

: 144599-66-6
[(1-Benzyloxycarbonylamino-3-methyl-butyl)-methoxy-phosphinoyl]-acetic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: SOCl₂ / CH₂Cl₂ / 22 °C

2: 56 percent / Et₃N / CH₂Cl₂ / 22 °C

3: tetrahydrofuran / 1.) -78 deg C; 2.) 0 deg C

With thionyl chloride; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ja00327a046