(E)-3-[2-Butyl-3-(2-chloro-benzyl)-3H-imidazol-4-yl]-2-(2-methyl-benzyl)-acrylic acid methyl ester

Base Information

Chemical Name:(E)-3-[2-Butyl-3-(2-chloro-benzyl)-3H-imidazol-4-yl]-2-(2-methyl-benzyl)-acrylic acid methyl ester
CAS No.:134405-45-1
Molecular Formula:C₂₆H₂₉ClN₂O₂
Molecular Weight:436.981
Hs Code.:

Synonyms:(E)-3-[2-Butyl-3-(2-chloro-benzyl)-3H-imidazol-4-yl]-2-(2-methyl-benzyl)-acrylic acid methyl ester

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Chemical Property of (E)-3-[2-Butyl-3-(2-chloro-benzyl)-3H-imidazol-4-yl]-2-(2-methyl-benzyl)-acrylic acid methyl ester

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Technology Process of (E)-3-[2-Butyl-3-(2-chloro-benzyl)-3H-imidazol-4-yl]-2-(2-methyl-benzyl)-acrylic acid methyl ester

There total 8 articles about (E)-3-[2-Butyl-3-(2-chloro-benzyl)-3H-imidazol-4-yl]-2-(2-methyl-benzyl)-acrylic 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:

: 17849-38-6
2-Chlorobenzyl alcohol

: 134405-45-1
(E)-3-[2-Butyl-3-(2-chloro-benzyl)-3H-imidazol-4-yl]-2-(2-methyl-benzyl)-acrylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: diisopropylethylamine / CH₂Cl₂ / 0.33 h / -78 °C

2: CH₂Cl₂ / 18 h / Ambient temperature

3: 10percent aq. NaOH / methanol / 4 h / Heating

4: 93 percent / MnO₂ / CH₂Cl₂ / 19 h / Ambient temperature

5: 1.) NaH / 1.) DME, a) 50 deg C, 15 min, b) 25 deg C, 15 min, 2.) DME, a) 70 deg C, 2 h, b) 25 deg C, 18 h

With manganese(IV) oxide; sodium hydroxide; sodium hydride; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane;
DOI:10.1021/jm00099a013

Reference yield:

: 68283-19-2
2-n-butyl-4-(hydroxymethyl)imidazole

: 134405-45-1
(E)-3-[2-Butyl-3-(2-chloro-benzyl)-3H-imidazol-4-yl]-2-(2-methyl-benzyl)-acrylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 83 percent / 19 h / Ambient temperature

2: CH₂Cl₂ / 18 h / Ambient temperature

3: 10percent aq. NaOH / methanol / 4 h / Heating

4: 93 percent / MnO₂ / CH₂Cl₂ / 19 h / Ambient temperature

5: 1.) NaH / 1.) DME, a) 50 deg C, 15 min, b) 25 deg C, 15 min, 2.) DME, a) 70 deg C, 2 h, b) 25 deg C, 18 h

With manganese(IV) oxide; sodium hydroxide; sodium hydride; In methanol; dichloromethane;
DOI:10.1021/jm00099a013

Reference yield:

: 133486-41-6
1-acetyl-4-acetoxymethyl-2-n-butylimidazole

: 134405-45-1
(E)-3-[2-Butyl-3-(2-chloro-benzyl)-3H-imidazol-4-yl]-2-(2-methyl-benzyl)-acrylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: CH₂Cl₂ / 18 h / Ambient temperature

2: 10percent aq. NaOH / methanol / 4 h / Heating

3: 93 percent / MnO₂ / CH₂Cl₂ / 19 h / Ambient temperature

4: 1.) NaH / 1.) DME, a) 50 deg C, 15 min, b) 25 deg C, 15 min, 2.) DME, a) 70 deg C, 2 h, b) 25 deg C, 18 h

With manganese(IV) oxide; sodium hydroxide; sodium hydride; In methanol; dichloromethane;
DOI:10.1021/jm00099a013