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2-Chloroethyl methyl sulfide → HCID 178503836, 화합물

HRID 1578100
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인쇄 미리보기

반응식

HRID 1578100 반응식
Cl[CH2:2][CH2:3][S:4][CH3:5].[C:6]([C:10]1[N:14]=[C:13]([SH:15])[NH:12][N:11]=1)([CH3:9])([CH3:8])[CH3:7]>CC[O-].[Na+]>[C:6]([C:10]1[N:14]=[C:13]([S:15][CH2:2][CH2:3][S:4][CH3:5])[NH:12][N:11]=1)([CH3:9])([CH3:8])[CH3:7]
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참가 물질

4

반응물 2

HCID 109652-Chloroethyl methyl sulfideHCID 178441989HCID 178441989, 화합물

생성물 1

HCID 178503836HCID 178503836, 화합물

시약·촉매·용매 1

HCID 2723922Sodium ethoxide용매

반응 조건

온도
80 °C

실험 절차

15 g of 2-chloroethyl-methylsulfide are added dropwise to a solution of 15.7 g of 3-tert-butyl-5-mercapto-1,2,4-triazole in ethanolic sodium ethylate (2.3 g of sodium in 300 ml of ethanol). The reaction mixture is stirred for 2 hours at 80° C., then cooled and filtered. The solvent is removed in vacuo and the residue is taken up in 300 ml of chloroform and extracted with 100 ml of water. The solvent is removed by distillation and the crude product is washed with cold petroleum ether, yielding 3-tert-butyl-5-(2-methylthioethylthio)-1,2,4-triazole of the formula ##STR5## with a melting point of 114°-116° C.

후처리

  1. temperaturecooled
  2. filtrationfiltered
  3. customThe solvent is removed in vacuo
  4. extractionextracted with 100 ml of water
  5. customThe solvent is removed by distillation
  6. washthe crude product is washed with cold petroleum ether

출처 및 근거

ORD 기록
ord-04a01d0864e346eb9fa597c2089c9c57
출처 데이터셋
uspto-grants-1981_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04291043

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