(Z)-2-[4-[1-(4-(benzyloxy)phenyl)-2-phenyl-1-butenyl]phenoxy]acetic acid benzyl ester

Base Information

Chemical Name:(Z)-2-[4-[1-(4-(benzyloxy)phenyl)-2-phenyl-1-butenyl]phenoxy]acetic acid benzyl ester
CAS No.:440646-12-8
Molecular Formula:C₃₈H₃₄O₄
Molecular Weight:554.686
Hs Code.:

Synonyms:(Z)-2-[4-[1-(4-(benzyloxy)phenyl)-2-phenyl-1-butenyl]phenoxy]acetic acid benzyl ester

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Chemical Property of (Z)-2-[4-[1-(4-(benzyloxy)phenyl)-2-phenyl-1-butenyl]phenoxy]acetic acid benzyl ester

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Technology Process of (Z)-2-[4-[1-(4-(benzyloxy)phenyl)-2-phenyl-1-butenyl]phenoxy]acetic acid benzyl ester

There total 7 articles about (Z)-2-[4-[1-(4-(benzyloxy)phenyl)-2-phenyl-1-butenyl]phenoxy]acetic acid benzyl 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: 86.0%

: 440646-09-3
(E)-1-[4-(benzyloxy)phenyl]-1-(4-hydroxyphenyl)-2-phenylbut-1-ene

: 5437-45-6
Benzyl bromoacetate

: 440646-12-8
(Z)-2-[4-[1-(4-(benzyloxy)phenyl)-2-phenyl-1-butenyl]phenoxy]acetic acid benzyl ester

Guidance literature:: With potassium carbonate; In acetone; for 1h; Heating;
DOI:10.1021/jo0255328

Reference yield:

: 611-99-4
4,4'-Dihydroxybenzophenone

: 440646-12-8
(Z)-2-[4-[1-(4-(benzyloxy)phenyl)-2-phenyl-1-butenyl]phenoxy]acetic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 72 percent / K₂CO₃ / dimethylformamide / 48 h / 60 °C

2: 87 percent / tetrabutylammonuim hydrogen sulfate; sodium hidroxide / CH₂Cl₂ / 20 °C

3: TiCl₄; zinc powder / tetrahydrofuran / Heating

4: 100 percent / MeONa / dimethylformamide / 1.5 h

5: 86 percent / K₂CO₃ / acetone / 1 h / Heating

With sodium hydroxide; sodium methylate; tetra(n-butyl)ammonium hydrogensulfate; titanium tetrachloride; potassium carbonate; zinc; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetone; 3: McMurry reaction;
DOI:10.1021/jo0255328

Reference yield:

: 100-39-0
benzyl bromide

: 440646-12-8
(Z)-2-[4-[1-(4-(benzyloxy)phenyl)-2-phenyl-1-butenyl]phenoxy]acetic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 72 percent / K₂CO₃ / dimethylformamide / 48 h / 60 °C

2: 87 percent / tetrabutylammonuim hydrogen sulfate; sodium hidroxide / CH₂Cl₂ / 20 °C

3: TiCl₄; zinc powder / tetrahydrofuran / Heating

4: 100 percent / MeONa / dimethylformamide / 1.5 h

5: 86 percent / K₂CO₃ / acetone / 1 h / Heating

With sodium hydroxide; sodium methylate; tetra(n-butyl)ammonium hydrogensulfate; titanium tetrachloride; potassium carbonate; zinc; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetone; 3: McMurry reaction;
DOI:10.1021/jo0255328