(E)-cinnamyl benzoyloxycarbamate

Base Information

Chemical Name:(E)-cinnamyl benzoyloxycarbamate
CAS No.:1424055-53-7
Molecular Formula:C₁₇H₁₅NO₄
Molecular Weight:297.31
Hs Code.:

Synonyms:(E)-cinnamyl benzoyloxycarbamate

Suppliers and Price of (E)-cinnamyl benzoyloxycarbamate

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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 (E)-cinnamyl benzoyloxycarbamate

Chemical Property:

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Technology Process of (E)-cinnamyl benzoyloxycarbamate

There total 2 articles about (E)-cinnamyl benzoyloxycarbamate 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:

: 4407-36-7
(2E)-3-phenyl-2-propen-1-ol

: 1424055-53-7
(E)-cinnamyl benzoyloxycarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: acetonitrile / 20 °C

2: triethylamine / 0 °C

With triethylamine; In acetonitrile;
DOI:10.1021/ja311923z

Reference yield:

: 98-88-4
benzoyl chloride

: 103723-92-8
(E)-3-phenylprop-2-enyl N-hydroxycarbamate

: 1424055-53-7
(E)-cinnamyl benzoyloxycarbamate

Guidance literature:: With triethylamine; at 0 ℃;
DOI:10.1021/ja311923z

Reference yield: 89.0%

: 1424055-53-7
(E)-cinnamyl benzoyloxycarbamate

: 129217-18-1
(2-oxooxazolidin-4-yl)(phenyl)methyl benzoate

Guidance literature:: With 1,10-Phenanthroline; potassium ferrocyanide; In acetonitrile; at 70 ℃; for 4h; Reagent/catalyst; diastereoselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1021/ja311923z