2--4-benzylidene-5-oxazolone

Base Information

Chemical Name:2--4-benzylidene-5-oxazolone
CAS No.:87483-08-7
Molecular Formula:C₂₁H₁₉NO₄
Molecular Weight:349.386
Hs Code.:

2-<o-(tert-Butoxycarbonyl)phenyl>-4-benzylidene-5-oxazolone

Synonyms:2--4-benzylidene-5-oxazolone

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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 2--4-benzylidene-5-oxazolone

Chemical Property:

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Technology Process of 2--4-benzylidene-5-oxazolone

There total 1 articles about 2--4-benzylidene-5-oxazolone 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: 49.0%

: 87483-07-6
N-glycine

: 100-52-7
benzaldehyde

: 87483-08-7
2--4-benzylidene-5-oxazolone

Guidance literature:: With sodium acetate; acetic anhydride; for 24h; Ambient temperature;
DOI:10.1021/jo00172a061

Reference yield: 94.0%

: 87483-08-7
2--4-benzylidene-5-oxazolone

: 87483-09-8
(Z)-2-(o-Carboxyphenyl)-4-benzylidene-5-oxazolone

Guidance literature:: With trifluoroacetic acid; In dichloromethane; for 2h; Ambient temperature;
DOI:10.1021/jo00172a061

Reference yield:

: 87483-08-7
2--4-benzylidene-5-oxazolone

: 87483-11-2
(Z)-1-Phenyl-5--6-oxo-4-azaspiro<2.4>hept-4-en-7-one

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / CF₃COOH / CH₂Cl₂ / 2 h / Ambient temperature

2: 33 percent / CH₂Cl₂; diethyl ether / 24 h / Ambient temperature

With trifluoroacetic acid; In diethyl ether; dichloromethane;
DOI:10.1021/jo00172a061