[4-(1-Benzyloxycarbonylamino-2-trimethylsilanyl-ethyl)-phenoxy]-acetic acid benzyl ester

Base Information

Chemical Name:[4-(1-Benzyloxycarbonylamino-2-trimethylsilanyl-ethyl)-phenoxy]-acetic acid benzyl ester
CAS No.:1026348-22-0
Molecular Formula:C₂₈H₃₃NO₅Si
Molecular Weight:491.659
Hs Code.:

Synonyms:[4-(1-Benzyloxycarbonylamino-2-trimethylsilanyl-ethyl)-phenoxy]-acetic acid benzyl ester

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Chemical Property of [4-(1-Benzyloxycarbonylamino-2-trimethylsilanyl-ethyl)-phenoxy]-acetic acid benzyl ester

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Technology Process of [4-(1-Benzyloxycarbonylamino-2-trimethylsilanyl-ethyl)-phenoxy]-acetic acid benzyl ester

There total 4 articles about [4-(1-Benzyloxycarbonylamino-2-trimethylsilanyl-ethyl)-phenoxy]-acetic 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:

: 4397-53-9
p-benzyloxybenzaldehyde

: 1026348-22-0
[4-(1-Benzyloxycarbonylamino-2-trimethylsilanyl-ethyl)-phenoxy]-acetic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1) lithium bis(trimethylsilyl)amide / 1) a) hexane, THF, 0 deg C, 30 min, 2) hexane, THF, pentane, a) 0 deg C, 2 h, b) room temperature, 30 min

2: 90 percent / hydrogen / 10percent Pd/C / methanol / 2585.7 Torr

3: 88 percent / diisopropylethylamine / CH₂Cl₂; dimethylformamide / 5 h / Ambient temperature

4: 1) NaH / 1) DMF, 0 deg C, 30 min, 2) DMF, room temperature, 5 h

With hydrogen; sodium hydride; N-ethyl-N,N-diisopropylamine; lithium hexamethyldisilazane; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo00061a049

Reference yield:

: 4-<1-amino-2-(trimethylsilyl)ethyl>phenyl benzyl ether hydrochloride

: 1026348-22-0
[4-(1-Benzyloxycarbonylamino-2-trimethylsilanyl-ethyl)-phenoxy]-acetic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / hydrogen / 10percent Pd/C / methanol / 2585.7 Torr

2: 88 percent / diisopropylethylamine / CH₂Cl₂; dimethylformamide / 5 h / Ambient temperature

3: 1) NaH / 1) DMF, 0 deg C, 30 min, 2) DMF, room temperature, 5 h

With hydrogen; sodium hydride; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo00061a049

Reference yield:

: 4-<1-amino-2-(trimethylsilyl)ethyl>phenol hydrochloride

: 1026348-22-0
[4-(1-Benzyloxycarbonylamino-2-trimethylsilanyl-ethyl)-phenoxy]-acetic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / diisopropylethylamine / CH₂Cl₂; dimethylformamide / 5 h / Ambient temperature

2: 1) NaH / 1) DMF, 0 deg C, 30 min, 2) DMF, room temperature, 5 h

With sodium hydride; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo00061a049