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Water → 3-Methoxymethyl-5-[(4-methylphenyl)-sulfonyl]-1,2,4-thiadiazole

HRID 1416320
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HRID 1416320 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([C:11]#[N:12])(=[O:10])=[O:9])=[CH:4][CH:3]=1.[CH3:13][O:14][CH2:15][C:16]1OC(=O)[S:18][N:17]=1.O>CCCCCCCCCCCC>[CH3:13][O:14][CH2:15][C:16]1[N:12]=[C:11]([S:8]([C:5]2[CH:4]=[CH:3][C:2]([CH3:1])=[CH:7][CH:6]=2)(=[O:10])=[O:9])[S:18][N:17]=1
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참가 물질

5

반응물 3

HCID 962WaterHCID 87946p-Toluenesulphonyl cyanideHCID 218503335-Methoxymethyl-1,3,4-oxathiazol-2-one

생성물 1

HCID 218503733-Methoxymethyl-5-[(4-methylphenyl)-sulfonyl]-1,2,4-thiadiazole

시약·촉매·용매 1

HCID 8182Dodecane용매

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온도
150 °C

실험 절차

4-Methylbenzenesulfonyl cyanide (16.26 g) was added to an emulsion of 5-methoxymethyl-1,3,4-oxathiazol-2-one (6.6 g) in dodecane (60 cm3). The reaction mixture was stirred and heated at 150° C. for 18 hours, then cooled. Water was added and the product extracted into ethyl acetate. The combined organic phases were dried (MgSO4) and ethyl acetate was removed by evaporation under reduced pressure. The residue separated into a brown liquid and a clear dodecane layer which was removed and discarded. Chromatography of the brown liquid on silica gel (Sorbsil C30) using 3:7 ethyl acetate:hexane as eluant give a pale orange oil which solidified on standing (6.94 g). M+ =284; 1H NMR: δ 2.40(3H,s); 3.45(3H,s); 4.7(2H,s); 7.4(2H,d); 8.0(2H,d); (mp 43.4-45-4° C.).

후처리

  1. temperaturecooled
  2. extractionthe product extracted into ethyl acetate
  3. dry with materialThe combined organic phases were dried (MgSO4) and ethyl acetate
  4. customwas removed by evaporation under reduced pressure
  5. customThe residue separated into a brown liquid
  6. customa clear dodecane layer which was removed
  7. customhexane as eluant give a pale orange oil which
  8. custom(mp 43.4-45-4° C.)

출처 및 근거

ORD 기록
ord-1870628798e8491aad2820e66a60204b
출처 데이터셋
uspto-grants-1999_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05912243

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