2-<2-<3-(1-propenyl)>-3-<3-<5-(benzyloxy)-2-ethyl-4-(4-fluorophenyl)phenoxy>propoxy>benzoyl>benzoic acid methyl ester

Base Information

Chemical Name:2-<2-<3-(1-propenyl)>-3-<3-<5-(benzyloxy)-2-ethyl-4-(4-fluorophenyl)phenoxy>propoxy>benzoyl>benzoic acid methyl ester
CAS No.:152610-15-6
Molecular Formula:C₄₂H₃₉FO₆
Molecular Weight:658.766
Hs Code.:

Synonyms:2-<2-<3-(1-propenyl)>-3-<3-<5-(benzyloxy)-2-ethyl-4-(4-fluorophenyl)phenoxy>propoxy>benzoyl>benzoic acid methyl ester

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Chemical Property of 2-<2-<3-(1-propenyl)>-3-<3-<5-(benzyloxy)-2-ethyl-4-(4-fluorophenyl)phenoxy>propoxy>benzoyl>benzoic acid methyl ester

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Technology Process of 2-<2-<3-(1-propenyl)>-3-<3-<5-(benzyloxy)-2-ethyl-4-(4-fluorophenyl)phenoxy>propoxy>benzoyl>benzoic acid methyl ester

There total 10 articles about 2-<2-<3-(1-propenyl)>-3-<3-<5-(benzyloxy)-2-ethyl-4-(4-fluorophenyl)phenoxy>propoxy>benzoyl>benzoic acid methyl 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: 65.0%

: 152120-11-1
4-(benzyloxy)-5-(4-fluorophenyl)-2-(3-iodopropoxy)ethylbenzene

: 152610-14-5
2-<3-hydroxy-2-<3-(1-propenyl)>benzoyl>benzoic acid methyl ester

: 152610-15-6
2-<2-<3-(1-propenyl)>-3-<3-<5-(benzyloxy)-2-ethyl-4-(4-fluorophenyl)phenoxy>propoxy>benzoyl>benzoic acid methyl ester

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; for 24h; Ambient temperature;
DOI:10.1021/jm00022a006

Reference yield:

: 85-44-9
phthalic anhydride

: 152610-15-6
2-<2-<3-(1-propenyl)>-3-<3-<5-(benzyloxy)-2-ethyl-4-(4-fluorophenyl)phenoxy>propoxy>benzoyl>benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) n-BuLi / 1.) THF, -70 deg C, 1 h, 2.) THF, from -70 deg C to RT

2: 100 percent / HCl(g) / 18 h / Ambient temperature

3: 54 percent / 30 h / 175 °C

4: 65 percent / K₂CO₃ / dimethylformamide / 24 h / Ambient temperature

With hydrogenchloride; n-butyllithium; potassium carbonate; In N,N-dimethyl-formamide;
DOI:10.1021/jm00022a006

Reference yield:

: 29682-12-0
1-[4-(benzyloxy)-2-hydroxyphenyl]ethanone

: 152610-15-6
2-<2-<3-(1-propenyl)>-3-<3-<5-(benzyloxy)-2-ethyl-4-(4-fluorophenyl)phenoxy>propoxy>benzoyl>benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 82 percent / K₂CO₃ / dimethylsulfoxide; butan-2-one / 24 h / Heating

2: 69 percent / trifluoroacetic acid, triethylsilane / CCl₄ / 1.5 h / Ambient temperature

3: 73 percent / N-bromosuccinimide / CCl₄ / 6 h / Ambient temperature

4: 84 percent / Pd(PPh₃)4, aq. Na₂CO₃ / ethanol; benzene / 16 h / Heating

5: 100 percent / NaI / butan-2-one / 6 h / Heating

6: 65 percent / K₂CO₃ / dimethylformamide / 24 h / Ambient temperature

With triethylsilane; N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate; potassium carbonate; trifluoroacetic acid; sodium iodide; In tetrachloromethane; ethanol; dimethyl sulfoxide; N,N-dimethyl-formamide; butanone; benzene;
DOI:10.1021/jm00022a006