N-benzyl-8-bromo-6,7,8,9-tetrahydro-9-oxo-5H-benzocycloheptene-5-carboxamide

Base Information

Chemical Name:N-benzyl-8-bromo-6,7,8,9-tetrahydro-9-oxo-5H-benzocycloheptene-5-carboxamide
CAS No.:105166-26-5
Molecular Formula:C₁₉H₁₈BrNO₂
Molecular Weight:372.261
Hs Code.:

Synonyms:N-benzyl-8-bromo-6,7,8,9-tetrahydro-9-oxo-5H-benzocycloheptene-5-carboxamide

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Chemical Property of N-benzyl-8-bromo-6,7,8,9-tetrahydro-9-oxo-5H-benzocycloheptene-5-carboxamide

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Technology Process of N-benzyl-8-bromo-6,7,8,9-tetrahydro-9-oxo-5H-benzocycloheptene-5-carboxamide

There total 6 articles about N-benzyl-8-bromo-6,7,8,9-tetrahydro-9-oxo-5H-benzocycloheptene-5-carboxamide 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: 82.0%

: 105166-25-4
N-benzyl-6,7,8,9-tetrahydro-9-oxo-5H-benzocycloheptene-5-carboxamide

: 105166-26-5
N-benzyl-8-bromo-6,7,8,9-tetrahydro-9-oxo-5H-benzocycloheptene-5-carboxamide

Guidance literature:: With bromine; In acetic acid; for 0.5h; Ambient temperature;

Reference yield:

: 20343-33-3
6,7,8,9-tetrahydro-9-oxo-5H-benzocycloheptene-5-carboxylic acid

: 105166-26-5
N-benzyl-8-bromo-6,7,8,9-tetrahydro-9-oxo-5H-benzocycloheptene-5-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: thionyl chloride / CH₂Cl₂ / 1 h / Heating

2: CH₂Cl₂ / 0.05 h / 0 °C

3: 82 percent / bromine / acetic acid / 0.5 h / Ambient temperature

With thionyl chloride; bromine; In dichloromethane; acetic acid;

Reference yield:

: 72472-29-8
9-bromo-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-one

: 105166-26-5
N-benzyl-8-bromo-6,7,8,9-tetrahydro-9-oxo-5H-benzocycloheptene-5-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: 60 percent / dimethylsulfoxide / 4 h / 75 - 80 °C

2: 57 percent / potassium hydroxide / aq. ethanol / 24 h / Heating

3: thionyl chloride / CH₂Cl₂ / 1 h / Heating

4: CH₂Cl₂ / 0.05 h / 0 °C

5: 82 percent / bromine / acetic acid / 0.5 h / Ambient temperature

With potassium hydroxide; thionyl chloride; bromine; In ethanol; dichloromethane; acetic acid; dimethyl sulfoxide;