[4-(1-Benzylcarbamoyl-3,3-diethyl-4-oxo-azetidin-2-yloxy)-phenyl]-acetic acid tert-butyl ester

Base Information

Chemical Name:[4-(1-Benzylcarbamoyl-3,3-diethyl-4-oxo-azetidin-2-yloxy)-phenyl]-acetic acid tert-butyl ester
CAS No.:1027034-44-1
Molecular Formula:C₂₇H₃₄N₂O₅
Molecular Weight:466.577
Hs Code.:

Synonyms:[4-(1-Benzylcarbamoyl-3,3-diethyl-4-oxo-azetidin-2-yloxy)-phenyl]-acetic acid tert-butyl ester

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Chemical Property of [4-(1-Benzylcarbamoyl-3,3-diethyl-4-oxo-azetidin-2-yloxy)-phenyl]-acetic acid tert-butyl ester

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Technology Process of [4-(1-Benzylcarbamoyl-3,3-diethyl-4-oxo-azetidin-2-yloxy)-phenyl]-acetic acid tert-butyl ester

There total 5 articles about [4-(1-Benzylcarbamoyl-3,3-diethyl-4-oxo-azetidin-2-yloxy)-phenyl]-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:

: 142935-27-1
3,3-diethyl-4-<<4-<<(1,1-dimethylethoxy)carbonyl>methyl>phenyl>oxy>-2-azetidinone

: 3173-56-6
benzyl isothiocyanate

: 1027034-44-1
[4-(1-Benzylcarbamoyl-3,3-diethyl-4-oxo-azetidin-2-yloxy)-phenyl]-acetic acid tert-butyl ester

Guidance literature:: With dmap; triethylamine; In dichloromethane; for 2h; Ambient temperature;
DOI:10.1021/jm00058a015

Reference yield:

: 156-38-7
4-hydroxyphenylacetate

: 1027034-44-1
[4-(1-Benzylcarbamoyl-3,3-diethyl-4-oxo-azetidin-2-yloxy)-phenyl]-acetic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: N,N'-diisopropyl-O-tert-butylisourea / Ambient temperature

2: 1.) 2.5 N aq. NaOH / 1.) acetone, 0 deg C, 20 min, 2.) acetone, H₂O, RT, 20 h

3: Et₃N, 4-(dimethylamino)pyridine / CH₂Cl₂ / 2 h / Ambient temperature

With dmap; sodium hydroxide; 2-tert-butyl-1,3-diisopropylisourea; triethylamine; In dichloromethane;
DOI:10.1021/jm00058a015

Reference yield:

: 16010-88-1
tert-butyl 2-(4-hydroxyphenyl)acetate

: 1027034-44-1
[4-(1-Benzylcarbamoyl-3,3-diethyl-4-oxo-azetidin-2-yloxy)-phenyl]-acetic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) 2.5 N aq. NaOH / 1.) acetone, 0 deg C, 20 min, 2.) acetone, H₂O, RT, 20 h

2: Et₃N, 4-(dimethylamino)pyridine / CH₂Cl₂ / 2 h / Ambient temperature

With dmap; sodium hydroxide; triethylamine; In dichloromethane;
DOI:10.1021/jm00058a015