(Z)-3-(butylamino)-3-oxo-1-phenylprop-1-en-2-yl 2-(3-methoxyphenyl)acetate

Base Information

Chemical Name:(Z)-3-(butylamino)-3-oxo-1-phenylprop-1-en-2-yl 2-(3-methoxyphenyl)acetate
CAS No.:1592424-66-2
Molecular Formula:C₂₂H₂₅NO₄
Molecular Weight:367.445
Hs Code.:

Synonyms:(Z)-3-(butylamino)-3-oxo-1-phenylprop-1-en-2-yl 2-(3-methoxyphenyl)acetate

Suppliers and Price of (Z)-3-(butylamino)-3-oxo-1-phenylprop-1-en-2-yl 2-(3-methoxyphenyl)acetate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (Z)-3-(butylamino)-3-oxo-1-phenylprop-1-en-2-yl 2-(3-methoxyphenyl)acetate

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Technology Process of (Z)-3-(butylamino)-3-oxo-1-phenylprop-1-en-2-yl 2-(3-methoxyphenyl)acetate

There total 2 articles about (Z)-3-(butylamino)-3-oxo-1-phenylprop-1-en-2-yl 2-(3-methoxyphenyl)acetate 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: 88.0%

: 2769-64-4
n-butyl isonitrile

: 1798-09-0
m-methoxyphenylacetic acid

: 3282-32-4
2-diazo-acetophenone

: 1592424-66-2
(Z)-3-(butylamino)-3-oxo-1-phenylprop-1-en-2-yl 2-(3-methoxyphenyl)acetate

Guidance literature:: In dichloromethane; at 20 ℃; Sealed tube; Inert atmosphere; Irradiation;
DOI:10.1021/acs.joc.1c00278

Reference yield:

: 2769-64-4
n-butyl isonitrile

: 1798-09-0
m-methoxyphenylacetic acid

: 3282-32-4
2-diazo-acetophenone

: 1592424-66-2
(Z)-3-(butylamino)-3-oxo-1-phenylprop-1-en-2-yl 2-(3-methoxyphenyl)acetate

: 1592424-86-6
(E)-3-(butylamino)-3-oxo-1-phenylprop-1-en-2-yl 2-(3-methoxyphenyl)acetate

Guidance literature:: In acetone; at 20 ℃; for 3h; Overall yield = 68 %; stereoselective reaction; Inert atmosphere; UV-irradiation;
DOI:10.1021/jo500535f