(E)-2-phenylethenyl propanoate

Base Information

Chemical Name:(E)-2-phenylethenyl propanoate
CAS No.:38180-75-5
Molecular Formula:C₁₁H₁₂O₂
Molecular Weight:176.215
Hs Code.:

Synonyms:

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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)-2-phenylethenyl propanoate

Chemical Property:

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Technology Process of (E)-2-phenylethenyl propanoate

There total 6 articles about (E)-2-phenylethenyl propanoate 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: 58.0%

: 802294-64-0,79-09-4
propionic acid

: 536-74-3
phenylacetylene

: 33603-01-9,38180-75-5
(Z)-2-phenylethenyl propanoate

: 38180-75-5,33603-01-9
(E)-2-phenylethenyl propanoate

: 79408-80-3
1-phenylethenyl propanoate

Guidance literature:: [RuCl(η²-O2CCH2CH3)(CO)(PPh3)2]; In benzene; for 24h; Further Variations:; Catalysts; Reagents; Product distribution; Heating;
DOI:10.1016/S0022-328X(00)00027-9

Reference yield: 58.0%

: 802294-64-0,79-09-4
propionic acid

: 536-74-3
phenylacetylene

: 33603-01-9,38180-75-5
(Z)-2-phenylethenyl propanoate

: 38180-75-5,33603-01-9
(E)-2-phenylethenyl propanoate

: 79408-80-3
1-phenylethenyl propanoate

Guidance literature:: [RuCl(η²-O2CCH2CH3)(CO)(PPh3)2]; In benzene; for 24h; Further Variations:; Catalysts; Reagents; Product distribution; Heating;
DOI:10.1016/S0022-328X(00)00027-9

Reference yield:

: 802294-64-0,79-09-4
propionic acid

: 536-74-3
phenylacetylene

: 33603-01-9,38180-75-5
(Z)-2-phenylethenyl propanoate

: 38180-75-5,33603-01-9
(E)-2-phenylethenyl propanoate

Guidance literature:: With C₂₄H₂₀B^(1-)*C₅₄H₅₀ClNP₄Ru⁽¹⁺⁾; In toluene; at 110 ℃; for 12h; optical yield given as %de; stereoselective reaction;
DOI:10.1016/j.jorganchem.2011.11.017