(E)-3-(4-chlorophenyl)allyl phenyl carbonate

Base Information

Chemical Name:(E)-3-(4-chlorophenyl)allyl phenyl carbonate
CAS No.:1054603-60-9
Molecular Formula:C₁₆H₁₃ClO₃
Molecular Weight:288.73
Hs Code.:

Synonyms:(E)-3-(4-chlorophenyl)allyl phenyl carbonate

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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)-3-(4-chlorophenyl)allyl phenyl carbonate

Chemical Property:

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Technology Process of (E)-3-(4-chlorophenyl)allyl phenyl carbonate

There total 1 articles about (E)-3-(4-chlorophenyl)allyl phenyl carbonate 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: 95.0%

: 24583-70-8
(E)-3-(p-chlorophenyl)prop-2-en-1-ol

: 1885-14-9
phenyl chloroformate

: 1054603-60-9
(E)-3-(4-chlorophenyl)allyl phenyl carbonate

Guidance literature:: With pyridine; In dichloromethane; at 20 ℃; for 12h;
DOI:10.1002/adsc.201000696

Reference yield: 82.0%

: 1054603-60-9
(E)-3-(4-chlorophenyl)allyl phenyl carbonate

: 403825-39-8
1-chloro-4-(1-phenoxyallyl)benzene

Guidance literature:: With C₃₁H₃₄N₅Ru⁽¹⁺⁾*F₆P^(1-); In tetrahydrofuran; at 25 ℃; for 12h; enantioselective reaction; Inert atmosphere; Schlenk technique;
DOI:10.1002/adsc.201500534

Reference yield:

: 1054603-62-1
cinnnamyl p-tolyl carbonate

: 1054603-60-9
(E)-3-(4-chlorophenyl)allyl phenyl carbonate

: 403825-39-8
1-chloro-4-(1-phenoxyallyl)benzene

: 1054603-72-3
1-chloro-4-(1-(p-tolyloxy)allyl)benzene

: 138621-80-4
1-phenyl-1-phenoxy-2-propene

: 512789-26-3,1054603-69-8,838828-13-0
1-methyl-4-((1-phenylallyl) oxy) benzene

Guidance literature:: With C₃₁H₃₄N₅Ru⁽¹⁺⁾*F₆P^(1-); In tetrahydrofuran; at 25 ℃; for 15h; Inert atmosphere; Schlenk technique;
DOI:10.1002/adsc.201500534