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Acetic Acid → 5-Bromo-7-fluoro-3,3-dimethylindolin-2-one

HRID 2250518
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HRID 2250518 반응식
[F:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:10]=1[NH:9][C:8](=[O:11])[C:7]2([CH3:13])[CH3:12].C(O)(=O)C.[Br:18]Br.S([O-])([O-])(=O)=S.[Na+].[Na+]>ClCCl>[Br:18][C:4]1[CH:5]=[C:6]2[C:10](=[C:2]([F:1])[CH:3]=1)[NH:9][C:8](=[O:11])[C:7]2([CH3:13])[CH3:12]
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참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 24408BromineHCID 24477Sodium ThiosulfateHCID 119764367-fluoro-3,3-dimethyloxindole

생성물 1

HCID 119764375-Bromo-7-fluoro-3,3-dimethylindolin-2-one수율 82%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

7-Fluoro-3,3-dimethyl-1,3-dihydro-2H-indol-2-one (4.1 g, 22.9 mmol) was dissolved in dichloromethane (100 mL) and acetic acid (2 mL) at room temperature. Bromine (1.2 mL, 23 mmol) was added and the solution allowed to stir for 24 hours. The reaction mixture was poured into sodium thiosulfate solution, extracted with diethyl ether, dried (MgSO4), evaporated and the crude product triturated with hexane to give 5-bromo-7-fluoro-3,3-dimethyl-1,3-dihydro-2H-indol-2-one (4.84 g, 82%): HRMS: calc'd for C10H9BrFNO, 256.9852; found (ESI, [M−H]−), 255.9781.

후처리

  1. customat room temperature
  2. extractionextracted with diethyl ether
  3. dry with materialdried (MgSO4)
  4. customevaporated
  5. customthe crude product triturated with hexane

출처 및 근거

ORD 기록
ord-2de8ad64d7844f0b9071c0b2204d01d2
출처 데이터셋
uspto-grants-2008_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07317037B2

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