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Water → 4-Bromo-2-chloro-6-methylbenzoic acid

HRID 2427644
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HRID 2427644 반응식
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([CH3:11])[CH:3]=1.[Cl:12]N1C(=O)CCC1=O.O>CN(C=O)C.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[Br:1][C:2]1[CH:3]=[C:4]([CH3:11])[C:5]([C:6]([OH:8])=[O:7])=[C:9]([Cl:12])[CH:10]=1
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참가 물질

6

반응물 3

HCID 962WaterHCID 31398ChlorosuccinimideHCID 995704-Bromo-2-methylbenzoic acid

생성물 1

HCID 566042464-Bromo-2-chloro-6-methylbenzoic acid

시약·촉매·용매 2

HCID 167845palladium(II) acetate촉매HCID 6228Dimethylformamide용매

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온도
100 °C

실험 절차

A mixture of 4-bromo-2-methyl-benzoic acid (6.45 g, 30 mmol,), N-chlorosuccinimide (4.67 g, 35 mmol), and palladium (II) acetate (0.675 g, 3 mmol) in dry DMF (35 mL) was heated under a nitrogen atmosphere at 100° C. for 36 h. After this time, the reaction mixture was cooled to ambient temperature and poured into water. The aqueous solution was extracted with ethyl acetate (2×100 mL) and the combined organic extracts washed with aqueous sodium thiosulphate (30 mL) and then brine (30 mL). The remaining organic solution was dried over anhydrous MgSO4, filtered, and concentrated to give 4-bromo-2-chloro-6-methyl-benzoic acid. The product was used without further purification.

후처리

  1. temperatureAfter this time, the reaction mixture was cooled to ambient temperature
  2. extractionThe aqueous solution was extracted with ethyl acetate (2×100 mL)
  3. washthe combined organic extracts washed with aqueous sodium thiosulphate (30 mL)
  4. dry with materialThe remaining organic solution was dried over anhydrous MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-29de73bbdc35461dba6dc6d934cf959e
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07968570B2

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