(E)-3-Phenyl-acrylic acid 1-tert-butyl-3-methyl-2-oxo-azetidin-3-yl ester

Base Information

Chemical Name:(E)-3-Phenyl-acrylic acid 1-tert-butyl-3-methyl-2-oxo-azetidin-3-yl ester
CAS No.:87750-91-2
Molecular Formula:C₁₇H₂₁NO₃
Molecular Weight:287.359
Hs Code.:

Synonyms:(E)-3-Phenyl-acrylic acid 1-tert-butyl-3-methyl-2-oxo-azetidin-3-yl ester

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Chemical Property of (E)-3-Phenyl-acrylic acid 1-tert-butyl-3-methyl-2-oxo-azetidin-3-yl ester

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Technology Process of (E)-3-Phenyl-acrylic acid 1-tert-butyl-3-methyl-2-oxo-azetidin-3-yl ester

There total 3 articles about (E)-3-Phenyl-acrylic acid 1-tert-butyl-3-methyl-2-oxo-azetidin-3-yl 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: 93.0%

: 87751-04-0
(E)-3-Phenyl-acrylic acid 1-tert-butylcarbamoyl-2-chloro-1-methyl-ethyl ester

: 87750-91-2
(E)-3-Phenyl-acrylic acid 1-tert-butyl-3-methyl-2-oxo-azetidin-3-yl ester

Guidance literature:: With cesium fluoride; N-benzyl-N,N,N-triethylammonium chloride; In tetrahydrofuran; for 1h; Heating;
DOI:10.1055/s-1983-30418

Reference yield:

: 119072-55-8,7188-38-7
tert-butylisonitrile

: 87750-91-2
(E)-3-Phenyl-acrylic acid 1-tert-butyl-3-methyl-2-oxo-azetidin-3-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / 15 h / Ambient temperature

2: 93 percent / CsF / benzyltriethylammonium chloride / tetrahydrofuran / 1 h / Heating

With cesium fluoride; N-benzyl-N,N,N-triethylammonium chloride; In tetrahydrofuran;
DOI:10.1055/s-1983-30418

Reference yield:

: 621-82-9
Cinnamic acid

: 87750-91-2
(E)-3-Phenyl-acrylic acid 1-tert-butyl-3-methyl-2-oxo-azetidin-3-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / 15 h / Ambient temperature

2: 93 percent / CsF / benzyltriethylammonium chloride / tetrahydrofuran / 1 h / Heating

With cesium fluoride; N-benzyl-N,N,N-triethylammonium chloride; In tetrahydrofuran;
DOI:10.1055/s-1983-30418