Benzyl--<1-(4-chlorbenzoyl)-5-methoxy-2-methylindol-3>>glykolat

Base Information

Chemical Name:Benzyl--<1-(4-chlorbenzoyl)-5-methoxy-2-methylindol-3>>glykolat
CAS No.:76812-74-3
Molecular Formula:C₃₀H₃₀ClNO₇
Molecular Weight:552.024
Hs Code.:

Benzyl-<O-<2-(2-hydroxyethoxy)ethyl>-<1-(4-chlorbenzoyl)-5-methoxy-2-methylindol-3>>glykolat

Synonyms:Benzyl--<1-(4-chlorbenzoyl)-5-methoxy-2-methylindol-3>>glykolat

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Chemical Property of Benzyl--<1-(4-chlorbenzoyl)-5-methoxy-2-methylindol-3>>glykolat

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Technology Process of Benzyl--<1-(4-chlorbenzoyl)-5-methoxy-2-methylindol-3>>glykolat

There total 4 articles about Benzyl--<1-(4-chlorbenzoyl)-5-methoxy-2-methylindol-3>>glykolat 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:

: 6260-97-5
(4-chlorophenyl)(5-methoxy-2-methyl-1H-indol-1-yl)methanone

: 76812-74-3
Benzyl--<1-(4-chlorbenzoyl)-5-methoxy-2-methylindol-3>>glykolat

Guidance literature:: Multi-step reaction with 3 steps

1: 81.9 percent / 5 h / 120 - 125 °C

2: SOCl₂ / CH₂Cl₂ / 2.5 h / 3 °C

3: CH₂Cl₂ / 2 h

With thionyl chloride; In dichloromethane;

Reference yield:

: 24285-32-3
Glyoxylsaeure-benzylester-benzyl-halbacetal

: 76812-74-3
Benzyl--<1-(4-chlorbenzoyl)-5-methoxy-2-methylindol-3>>glykolat

Guidance literature:: Multi-step reaction with 3 steps

1: 81.9 percent / 5 h / 120 - 125 °C

2: SOCl₂ / CH₂Cl₂ / 2.5 h / 3 °C

3: CH₂Cl₂ / 2 h

With thionyl chloride; In dichloromethane;

Reference yield:

: 70180-40-4
Benzyl<1-(4-chlorbenzoyl)-5-methoxy-2-methylindol-3>glykolat

: 76812-74-3
Benzyl--<1-(4-chlorbenzoyl)-5-methoxy-2-methylindol-3>>glykolat

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂ / CH₂Cl₂ / 2.5 h / 3 °C

2: CH₂Cl₂ / 2 h

With thionyl chloride; In dichloromethane;