Toluene → 2-Phenylthiomethyl-4-sec-butyl-6-methoxysaccharin

HRID 1768710노트

반응식

HRID 1768710 반응식
[CH:1]([C:5]1[CH:15]=[C:14]([O:16][CH3:17])[CH:13]=[C:12]2[C:6]=1[C:7](=[O:18])[NH:8][S:9]2(=[O:11])=[O:10])([CH2:3][CH3:4])[CH3:2].CC(C)([O-])C.[K+].C1([CH:31]([S:33]C(Cl)C2C=CC=CC=2)Cl)C=CC=CC=1.[C:42]1(C)[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC>[C:42]1([S:33][CH2:31][N:8]2[C:7](=[O:18])[C:6]3[C:12](=[CH:13][C:14]([O:16][CH3:17])=[CH:15][C:5]=3[CH:1]([CH2:3][CH3:4])[CH3:2])[S:9]2(=[O:10])=[O:11])[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1

참가 물질

6

반응물 4

HCID 1140TolueneHCID 20138743Phenylchloromethyl sulfideHCID 23665647Potassium tert-butoxideHCID 677845614-Sec-butyl-6-methoxysaccharin

생성물 1

HCID 677843062-Phenylthiomethyl-4-sec-butyl-6-methoxysaccharin수율 60%

시약·촉매·용매 1

HCID 74236Tetrabutylammonium Bromide촉매

실험 절차

A mixture of 4-sec-butyl-6-methoxysaccharin (3 g), toluene, potassium t-butoxide (1.4 g), and tetrabutylammonium bromide (0.4 g) was brought to reflux and phenylchloromethyl sulfide (1.8 mL) was added. The reaction mixture was refluxed for about 27 hours, the solvent was removed in vacuo, the reside was extracted with ethyl acetate, washed with brine and dried over Na2SO4. The solvent was removed in vacuo and the residue was purified by column chromatography on silica eluting with 10% ethyl acetate/hexane to afford 2.63 g (60%) of 2-phenylthiomethyl-4-sec-butyl-6-methoxysaccharin.

후처리

  1. temperatureto reflux
  2. temperatureThe reaction mixture was refluxed for about 27 hours
  3. customthe solvent was removed in vacuo
  4. extractionthe reside was extracted with ethyl acetate
  5. washwashed with brine
  6. dry with materialdried over Na2SO4
  7. customThe solvent was removed in vacuo
  8. customthe residue was purified by column chromatography on silica eluting with 10% ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-cc185564a7624f209e44b88300df2386
출처 데이터셋
uspto-grants-1995_01
특허 번호
US05378720

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