8-acetyl-4-[(3-bromophenyl)methyl]-2,2-difluoro-2H-1,4-benzoxazin-3(4H)-one

Base Information

Chemical Name:8-acetyl-4-[(3-bromophenyl)methyl]-2,2-difluoro-2H-1,4-benzoxazin-3(4H)-one
CAS No.:1268628-70-1
Molecular Formula:C₁₇H₁₂BrF₂NO₃
Molecular Weight:396.188
Hs Code.:

Synonyms:8-acetyl-4-[(3-bromophenyl)methyl]-2,2-difluoro-2H-1,4-benzoxazin-3(4H)-one

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Chemical Property of 8-acetyl-4-[(3-bromophenyl)methyl]-2,2-difluoro-2H-1,4-benzoxazin-3(4H)-one

Chemical Property:

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Technology Process of 8-acetyl-4-[(3-bromophenyl)methyl]-2,2-difluoro-2H-1,4-benzoxazin-3(4H)-one

There total 3 articles about 8-acetyl-4-[(3-bromophenyl)methyl]-2,2-difluoro-2H-1,4-benzoxazin-3(4H)-one 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:

: 823-78-9
meta-bromobenzyl bromide

: 1263413-32-6
8-acetyl-2,2-difluoro-2H-1,4-benzoxazin-3(4H)-one

: 1268628-70-1
8-acetyl-4-[(3-bromophenyl)methyl]-2,2-difluoro-2H-1,4-benzoxazin-3(4H)-one

Guidance literature:: With potassium carbonate; In acetonitrile; at 20 ℃; for 5h;

Reference yield:

: 1263413-27-9
8-bromo-2,2-difluoro-2H-1,4-benzoxazin-3(4H)-one

: 1268628-70-1
8-acetyl-4-[(3-bromophenyl)methyl]-2,2-difluoro-2H-1,4-benzoxazin-3(4H)-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-butyllithium / diethyl ether / -78 °C / Inert atmosphere

1.2: 1 h / -78 °C

1.3: pH 7

2.1: potassium carbonate / acetonitrile / 5 h / 20 °C

With n-butyllithium; potassium carbonate; In diethyl ether; acetonitrile;

Reference yield:

: 1263413-26-8
2-bromo-N-(3-bromo-2-hydroxyphenyl)-2,2-difluoroacetamide

: 1268628-70-1
8-acetyl-4-[(3-bromophenyl)methyl]-2,2-difluoro-2H-1,4-benzoxazin-3(4H)-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 2 h / 50 °C

2.1: n-butyllithium / diethyl ether / -78 °C / Inert atmosphere

2.2: 1 h / -78 °C

2.3: pH 7

3.1: potassium carbonate / acetonitrile / 5 h / 20 °C

With n-butyllithium; potassium carbonate; In diethyl ether; N,N-dimethyl-formamide; acetonitrile;