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Sulfuryl chloride → 2-Chloromethyl-4-sec-butyl-6-methoxysaccharin

HRID 1768711
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인쇄 미리보기

반응식

HRID 1768711 반응식
C1(S[CH2:8][N:9]2[C:19](=[O:20])[C:18]3[C:13](=[CH:14][C:15]([O:25][CH3:26])=[CH:16][C:17]=3[CH:21]([CH2:23][CH3:24])[CH3:22])[S:10]2(=[O:12])=[O:11])C=CC=CC=1.S(Cl)([Cl:30])(=O)=O>C(Cl)Cl>[Cl:30][CH2:8][N:9]1[C:19](=[O:20])[C:18]2[C:13](=[CH:14][C:15]([O:25][CH3:26])=[CH:16][C:17]=2[CH:21]([CH2:23][CH3:24])[CH3:22])[S:10]1(=[O:12])=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24648Sulfuryl chlorideHCID 677843062-Phenylthiomethyl-4-sec-butyl-6-methoxysaccharin

생성물 1

HCID 677844242-Chloromethyl-4-sec-butyl-6-methoxysaccharin

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 2-phenylthiomethyl-4-sec-butyl-6-methoxysaccharin (2.6 g) in CH2Cl2 (20 mL) was added sulfuryl chloride (0.7 mL). The mixture was stirred at ambient temperature overnight, and the solvent was removed in vacuo. The residue was treated with hexane and the mixture was sonicated for 6 hours. A precipitate formed with a collected by filtration to afford 1.33 g of 2-chloromethyl-4-sec-butyl-6-methoxysaccharin.

후처리

  1. customthe solvent was removed in vacuo
  2. additionThe residue was treated with hexane
  3. customthe mixture was sonicated for 6 hours
  4. customA precipitate formed with
  5. filtrationa collected by filtration

출처 및 근거

ORD 기록
ord-6b1992ad09da402982c2b314e2613c54
출처 데이터셋
uspto-grants-1995_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05378720

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