di-tert-butyl N-<(4-<oxymethyl>phenyl)carbamoyl>-L-glutamate

Base Information

Chemical Name:di-tert-butyl N-<(4-<oxymethyl>phenyl)carbamoyl>-L-glutamate
CAS No.:161803-05-0
Molecular Formula:C₃₇H₅₀N₂O₆Si
Molecular Weight:646.899
Hs Code.:

di-tert-butyl N-<(4-<<tert-butyldiphenylsilyl>oxymethyl>phenyl)carbamoyl>-L-glutamate

Synonyms:di-tert-butyl N-<(4-<oxymethyl>phenyl)carbamoyl>-L-glutamate

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Chemical Property of di-tert-butyl N-<(4-<oxymethyl>phenyl)carbamoyl>-L-glutamate

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Technology Process of di-tert-butyl N-<(4-<oxymethyl>phenyl)carbamoyl>-L-glutamate

There total 7 articles about di-tert-butyl N-<(4-<oxymethyl>phenyl)carbamoyl>-L-glutamate 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: 5.0%

: 32677-01-3
L-glutamic acid di-tert-butyl ester hydrochloride

: 113068-95-4
tert-butyldiphenylsilyl 4-oxymethylphenyl isocyanate

: tert-butyl 1-oxymethyl>phenyl)carbamoyl>-5-oxopyrrolidine-2-carboxylate

: 161803-05-0
di-tert-butyl N-<(4-<oxymethyl>phenyl)carbamoyl>-L-glutamate

Guidance literature:: With triethylamine; In tetrahydrofuran; for 3h; Ambient temperature;
DOI:10.1021/jm980425k

Reference yield:

: 619-73-8
4-nitrobenzyl chloride

: 161803-05-0
di-tert-butyl N-<(4-<oxymethyl>phenyl)carbamoyl>-L-glutamate

Guidance literature:: Multi-step reaction with 4 steps

1: 93 percent / imidazole / dimethylformamide / 5 h / Ambient temperature

2: 91 percent / ammonium formate / 10 percent Pd/C / ethanol / 1.5 h / 20 °C

3: 99 percent / Et₃N / toluene / 5 h / 70 °C

4: 63 percent / Et₃N / tetrahydrofuran / 3 h / Ambient temperature

With 1H-imidazole; ammonium formate; triethylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jm980425k

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 161803-05-0
di-tert-butyl N-<(4-<oxymethyl>phenyl)carbamoyl>-L-glutamate

Guidance literature:: Multi-step reaction with 4 steps

1: 93 percent / imidazole / dimethylformamide / 5 h / Ambient temperature

2: 91 percent / ammonium formate / 10 percent Pd/C / ethanol / 1.5 h / 20 °C

3: 99 percent / Et₃N / toluene / 5 h / 70 °C

4: 63 percent / Et₃N / tetrahydrofuran / 3 h / Ambient temperature

With 1H-imidazole; ammonium formate; triethylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jm980425k