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Boron tribromide → 2,2-Difluoro-1-(2-fluoro-4-hydroxyphenyl)ethan-1-one

HRID 216338
ノート
印刷プレビュー

反応式

HRID 216338 の反応式
[F:1][CH:2]([F:14])[C:3]([C:5]1[CH:10]=[CH:9][C:8]([O:11]C)=[CH:7][C:6]=1[F:13])=[O:4].B(Br)(Br)Br>C(Cl)Cl>[F:14][CH:2]([F:1])[C:3]([C:5]1[CH:10]=[CH:9][C:8]([OH:11])=[CH:7][C:6]=1[F:13])=[O:4]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 25134Boron tribromideHCID 866384912,2-Difluoro-1-(2-fluoro-4-methoxyphenyl)ethan-1-one

生成物 1

HCID 866384922,2-Difluoro-1-(2-fluoro-4-hydroxyphenyl)ethan-1-one

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

反応条件

温度
25 °C

実験手順

To 2,2-difluoro-1-(2-fluoro-4-methoxyphenyl)ethanone (45.0 g, 0.22 mol) in 400 mL of CH2Cl2 at −78° C. was added BBr3 (165.67 g, 0.66 mol) in 100 mL of CH2Cl2 dropwise. The resulting solution was stirred overnight at 25° C., and was quenched by dropwise addition of CH3OH (900 mL) at −30° C. and after stirring for 2 hours at −30° C. and for 1 hour at 25° C., the solvents were evaporated and the residue was purified by column chromatography (PE/EA 6:1) to afford 2,2-difluoro-1-(2-fluoro-4-hydroxyphenyl)ethanone as a solid.

後処理

  1. customwas quenched by dropwise addition of CH3OH (900 mL) at −30° C.
  2. stirringafter stirring for 2 hours at −30° C. and for 1 hour at 25° C.
  3. customthe solvents were evaporated
  4. customthe residue was purified by column chromatography (PE/EA 6:1)

出典と根拠

ORDレコード
ord-b38583673d8e4a07986fd872f6f200a2
出典データセット
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08193228B2

反応ノート

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