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Boron tribromide → 3-Fluoro-5-methoxyphenol

HRID 450918
ノート
印刷プレビュー

反応式

HRID 450918 の反応式
B(Br)(Br)Br.C[O:6][C:7]1[CH:8]=[C:9]([F:15])[CH:10]=[C:11]([O:13][CH3:14])[CH:12]=1>ClCCl>[F:15][C:9]1[CH:8]=[C:7]([OH:6])[CH:12]=[C:11]([O:13][CH3:14])[CH:10]=1
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 tribromide2 回HCID 27742571-Fluoro-3,5-dimethoxybenzene

生成物 1

HCID 521808213-Fluoro-5-methoxyphenol収率 54%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

Boron tribromide (1M in dichloromethane, 9 mL, 89.985 mmol) was added drop wise to an ice-cooled solution of 3,5-dimethoxy fluorobenzene (3 ml, 22.496 mmol) in dichloromethane (20 mL) and the mixture was stirred at 0° C. to room temperature for 4 hours. The solution was cooled to 0° C., further boron tribromide (4 ml, 44.992 mmol) was added and stirring continued, warming to room temperature for an additional 18 hours. The reaction was quenched with 0.88 ammonia solution and stirred at room temperature for 90 minutes. The organic layer was separated and extracted with 2N sodium hydroxide (30 ml), which was then acidified to pH1 by drop wise addition of concentrated hydrochloric acid. The aqueous layer was then re-extracted with dichloromethane (3×15 mL), the combined organic solution was dried over sodium sulfate and concentrated in vacuo to afford the title compound as a white solid in 54% yield, 1.72 g.

後処理

  1. stirringstirring
  2. temperaturewarming to room temperature for an additional 18 hours
  3. customThe reaction was quenched with 0.88 ammonia solution
  4. stirringstirred at room temperature for 90 minutes
  5. customThe organic layer was separated
  6. extractionextracted with 2N sodium hydroxide (30 ml), which
  7. additionwas then acidified to pH1 by drop wise addition of concentrated hydrochloric acid
  8. extractionThe aqueous layer was then re-extracted with dichloromethane (3×15 mL)
  9. dry with materialthe combined organic solution was dried over sodium sulfate
  10. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-9717dda9e6a94e8da824433951a22ecc
出典データセット
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08486992B2

反応ノート

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