Ethyl 3-(4-methoxy-2-bromobenzyl)-2-methyl-4-oxocyclohex-2-enecarboxylate

Base Information

Chemical Name:Ethyl 3-(4-methoxy-2-bromobenzyl)-2-methyl-4-oxocyclohex-2-enecarboxylate
CAS No.:155855-17-7
Molecular Formula:C₁₈H₂₁BrO₄
Molecular Weight:381.266
Hs Code.:

Synonyms:Ethyl 3-(4-methoxy-2-bromobenzyl)-2-methyl-4-oxocyclohex-2-enecarboxylate

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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 Ethyl 3-(4-methoxy-2-bromobenzyl)-2-methyl-4-oxocyclohex-2-enecarboxylate

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Technology Process of Ethyl 3-(4-methoxy-2-bromobenzyl)-2-methyl-4-oxocyclohex-2-enecarboxylate

There total 1 articles about Ethyl 3-(4-methoxy-2-bromobenzyl)-2-methyl-4-oxocyclohex-2-enecarboxylate 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%

: 487-51-4
4-carbethoxy-3-methyl-2-cyclohexen-1-one

: 54788-18-0
2-bromo-1-(bromomethyl)-4-methoxybenzene

: 155855-17-7
Ethyl 3-(4-methoxy-2-bromobenzyl)-2-methyl-4-oxocyclohex-2-enecarboxylate

Guidance literature:: With potassium tert-butylate; In tert-butyl alcohol; for 16h; Heating;
DOI:10.1021/jo00089a009

Reference yield: 80.0%

: 155855-17-7
Ethyl 3-(4-methoxy-2-bromobenzyl)-2-methyl-4-oxocyclohex-2-enecarboxylate

: 155855-22-4
2-(4-Methoxy-2-bromobenzyl)-3-methylcyclohex-2-en-1-one

Guidance literature:: With potassium hydroxide; In ethanol; for 14h; Heating;
DOI:10.1021/jo00089a009

Reference yield:

: 155855-17-7
Ethyl 3-(4-methoxy-2-bromobenzyl)-2-methyl-4-oxocyclohex-2-enecarboxylate

: 155855-26-8
2-(4-Methoxy-2-bromobenzyl)-3,3-dimethylcyclohexan-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / KOH / aq. ethanol / 14 h / Heating

2: 1.) CuLi, BF₃*Et₂O, 2.) BF₃*Et₂O / 1.) Et₂O, -50 deg C, 5 min, 2.) Et₂O, -30 deg C, 1.25 h

With potassium hydroxide; LiCu; boron trifluoride diethyl etherate; In ethanol;
DOI:10.1021/jo00089a009