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

HRID 1471558
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HRID 1471558 반응식
[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
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참가 물질

4

반응물 2

HCID 25134Boron tribromideHCID 231579156-Bromo-2-fluoro-3-methoxybenzaldehyde

생성물 1

HCID 534387996-Bromo-2-fluoro-3-hydroxybenzaldehyde수율 86%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-a6e9cfb14f5c417d846753de41535d88
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09012431B2

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