(Z)-3-phenylallyl benzoyloxycarbamate

Base Information

Chemical Name:(Z)-3-phenylallyl benzoyloxycarbamate
CAS No.:1424055-61-7
Molecular Formula:C₁₇H₁₅NO₄
Molecular Weight:297.31
Hs Code.:

Synonyms:(Z)-3-phenylallyl benzoyloxycarbamate

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Chemical Property of (Z)-3-phenylallyl benzoyloxycarbamate

Chemical Property:

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Technology Process of (Z)-3-phenylallyl benzoyloxycarbamate

There total 2 articles about (Z)-3-phenylallyl 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:

: 4510-34-3
(Z)-cinnamyl alcohol

: 1424055-61-7
(Z)-3-phenylallyl 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:

: 1366331-54-5
(Z)-3-phenylallyl hydroxycarbamate

: 98-88-4
benzoyl chloride

: 1424055-61-7
(Z)-3-phenylallyl benzoyloxycarbamate

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

Reference yield: 75.0%

: 1424055-61-7
(Z)-3-phenylallyl 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; diastereoselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1021/ja311923z