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Boron tribromide → 2,3-Difluoro-4-methyl-5-nitro-phenol

HRID 2065745
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HRID 2065745 반응식
COC(=O)[O:4][C:5]1[CH:10]=[C:9]([N+:11]([O-:13])=[O:12])[C:8]([CH3:14])=[C:7]([F:15])[C:6]=1[F:16].B(Br)(Br)Br>ClCCl>[F:16][C:6]1[C:7]([F:15])=[C:8]([CH3:14])[C:9]([N+:11]([O-:13])=[O:12])=[CH:10][C:5]=1[OH:4]
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참가 물질

4

반응물 2

HCID 25134Boron tribromideHCID 59377938Carbonic acid 2,3-difluoro-4-methyl-5-nitro-phenyl ester methyl ester

생성물 1

HCID 593779072,3-Difluoro-4-methyl-5-nitro-phenol수율 58%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A solution of carbonic acid 2,3-difluoro-4-methyl-5-nitro-phenyl ester methyl ester (2.3 g, 9.3 mmol) in dichloromethane (30 ml) was cooled to 0° C. in an ice bath, and 1.0M boron tribromide in dichloromethane (9.3 ml, 9.3 mmol) was added. The ice-bath was removed and the mixture was stirred at room temperature for 18 hours. Water was added and the mixture was extracted with EtOAc. The combined extracts were washed with water and brine, dried over MgSO4, filtered and concentrated to dryness under reduced pressure. Purification of the crude product by flash chromatography (hexanes:EtOAc 9:1) gave 1.02 g (58%) of 2,3-difluoro-4-methyl-5-nitro-phenol as a white solid.

후처리

  1. customThe ice-bath was removed
  2. additionWater was added
  3. extractionthe mixture was extracted with EtOAc
  4. washThe combined extracts were washed with water and brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated to dryness under reduced pressure
  8. customPurification of the crude product by flash chromatography (hexanes:EtOAc 9:1)

출처 및 근거

ORD 기록
ord-1ff7a241f398436b863a577cfe1db708
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08288552B2

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