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Boron tribromide → 6-Bromo-2-fluoro-3-hydroxybenzaldehyde

HRID 1255701
ノート
印刷プレビュー

反応式

HRID 1255701 の反応式
[Br:1][C:2]1[C:7]([CH:8]=[O:9])=[C:6]([F:10])[C:5]([O:11]C)=[CH:4][CH:3]=1.B(Br)(Br)Br>ClCCl>[Br:1][C:2]1[C:7]([CH:8]=[O:9])=[C:6]([F:10])[C:5]([OH:11])=[CH:4][CH:3]=1
参加物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 231579156-Bromo-2-fluoro-3-methoxybenzaldehyde

生成物 1

HCID 534387996-Bromo-2-fluoro-3-hydroxybenzaldehyde収率 86%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

A solution of 6-bromo-2-fluoro-3-methoxybenzaldehyde (2 g, 8.58 mmol) in dichloromethane (43 mL) under a nitrogen balloon was cooled to −78° C. in an acetone dry ice bath. 1 M boron tribromide solution in dichloromethane (9.5 mL) was added drop wise under nitrogen balloon. The reaction was stirred at room temperature overnight. The reaction was then put on an ice water bath and the excess boron tribromide was quenched with ice chips. Water was added and the solution was extracted with dichloromethane. The aqueous layer was extracted two times with dichloromethane. The organic layers were combined, washed with brine, dried over anhydrous sodium sulfate, and filtered. The solvent was removed under reduced pressure to give 6-bromo-2-fluoro-3-hydroxybenzaldehyde (1.61 g, 86% yield).

後処理

  1. customThe reaction was then put on an ice water bath
  2. customthe excess boron tribromide was quenched with ice chips
  3. additionWater was added
  4. extractionthe solution was extracted with dichloromethane
  5. extractionThe aqueous layer was extracted two times with dichloromethane
  6. washwashed with brine
  7. dry with materialdried over anhydrous sodium sulfate
  8. filtrationfiltered
  9. customThe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-9384f99a3c1044b3a0ba20fc43a12fc7
出典データセット
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08461135B2

反応ノート

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