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Methyl iodide → HCID 23295998, 화합물

HRID 1954285
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HRID 1954285 반응식
[Br:1][C:2]1[CH:7]=[C:6]([C:8](=[O:16])[C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[Cl:15])[CH:5]=[C:4]([CH2:17][CH3:18])[C:3]=1[OH:19].[C:20]([O-])([O-])=O.[K+].[K+].IC>>[Br:1][C:2]1[CH:7]=[C:6]([C:8](=[O:16])[C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[Cl:15])[CH:5]=[C:4]([CH2:17][CH3:18])[C:3]=1[O:19][CH3:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 23296012HCID 23296012, 화합물

생성물 1

HCID 23295998HCID 23295998, 화합물수율 66%

실험 절차

At ambient temperature, to a stirred mixture containing 2-bromo-4-(2-chlorobenzoyl)-6-ethylphenol (14.56 g, 42.82 mmol) and K2CO3 (8.90 g, 64.5 mmol) in N,N-DMF (11.6 mL) was added iodomethane (3.98 mL, 64.4 mmol). After 48 h, the reaction was quenched with H2O (300 mL) and extracted with hexane. The organic extracts were washed with H2O (2×100 mL), brine (1×100 mL), dried (Na2SO4) and concentrated. Purification on Biotage KP-Sil eluting with a 0, 2.5 & 5% EtOAc/hexane step gradient gave 10.0 g (66%) of the title compound. 1H NMR: consistent. mass spectrum (EI) m/z 352 (M+). Anal. Calcd. for C16H14BrClO2.0.2H2O: C, 53.79; H, 4.06; N, 0.00. Found: C, 53.89; H, 3.91; N, 0.08.

후처리

  1. customthe reaction was quenched with H2O (300 mL)
  2. extractionextracted with hexane
  3. washThe organic extracts were washed with H2O (2×100 mL), brine (1×100 mL)
  4. dry with materialdried (Na2SO4)
  5. concentrationconcentrated
  6. customPurification on Biotage KP-Sil
  7. washeluting with a 0, 2.5 & 5% EtOAc/hexane step gradient

출처 및 근거

ORD 기록
ord-274257dca60247aab7083d815cffed3f
출처 데이터셋
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06121271

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