(E)-3-(3,4-Bis-allyloxy-phenyl)-acrylic acid 1-allyloxycarbonyl-2-(3,4-bis-allyloxy-phenyl)-ethyl ester

Base Information

Chemical Name:(E)-3-(3,4-Bis-allyloxy-phenyl)-acrylic acid 1-allyloxycarbonyl-2-(3,4-bis-allyloxy-phenyl)-ethyl ester
CAS No.:179128-97-3
Molecular Formula:C₃₃H₃₆O₈
Molecular Weight:560.644
Hs Code.:

Synonyms:(E)-3-(3,4-Bis-allyloxy-phenyl)-acrylic acid 1-allyloxycarbonyl-2-(3,4-bis-allyloxy-phenyl)-ethyl ester

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Chemical Property of (E)-3-(3,4-Bis-allyloxy-phenyl)-acrylic acid 1-allyloxycarbonyl-2-(3,4-bis-allyloxy-phenyl)-ethyl ester

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Technology Process of (E)-3-(3,4-Bis-allyloxy-phenyl)-acrylic acid 1-allyloxycarbonyl-2-(3,4-bis-allyloxy-phenyl)-ethyl ester

There total 6 articles about (E)-3-(3,4-Bis-allyloxy-phenyl)-acrylic acid 1-allyloxycarbonyl-2-(3,4-bis-allyloxy-phenyl)-ethyl ester 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: 94.0%

: 179128-84-8
(E)-3-(3,4-bis(allyloxy)phenyl)acrylic acid

: 179128-90-6
3-(3,4-Bis-allyloxy-phenyl)-2-hydroxy-propionic acid allyl ester

: 179128-97-3
(E)-3-(3,4-Bis-allyloxy-phenyl)-acrylic acid 1-allyloxycarbonyl-2-(3,4-bis-allyloxy-phenyl)-ethyl ester

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In dichloromethane; at -20 - 20 ℃; for 12h;
DOI:10.1055/s-1996-4289

Reference yield:

: 68307-79-9
(Z)-3-(3,4-dihydroxyphenyl)-2-hydroxyacrylic acid

: 179128-97-3
(E)-3-(3,4-Bis-allyloxy-phenyl)-acrylic acid 1-allyloxycarbonyl-2-(3,4-bis-allyloxy-phenyl)-ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 100 percent / H₂ / 5percent Pd/C / ethanol / 3750.3 Torr

2: 1.) K₂CO₃, EtOH, 2.) KOH / 1.) reflux, 5 h, 2.) 12 h

3: 96 percent / tetrahydrofuran / 48 h / 50 °C

4: 94 percent / DMAP, DCC / CH₂Cl₂ / 12 h / -20 - 20 °C

With dmap; potassium hydroxide; ethanol; hydrogen; potassium carbonate; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1055/s-1996-4289

Reference yield:

: 71186-67-9
3,4-diallyloxybenzaldehyde

: 179128-97-3
(E)-3-(3,4-Bis-allyloxy-phenyl)-acrylic acid 1-allyloxycarbonyl-2-(3,4-bis-allyloxy-phenyl)-ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 81 percent / pyridine, piperidine / 1.) 80 deg C, 1 h, 2.) reflux, 1 h

2: 94 percent / DMAP, DCC / CH₂Cl₂ / 12 h / -20 - 20 °C

With piperidine; pyridine; dmap; dicyclohexyl-carbodiimide; In dichloromethane;
DOI:10.1055/s-1996-4289