Carbon Disulfide → Zinc Bis(2-trichloromethyl-3-oxazolidinecarbodithioate)

HRID 1283824

반응식

HRID 1283824 반응식
[Cl:1][C:2]([Cl:9])([Cl:8])[CH:3]1[NH:7][CH2:6][CH2:5][O:4]1.[C:10](=[S:12])=[S:11].C([O-])(=O)C.[Zn+2:17].C([O-])(=O)C>C(O)(C)C.O>[Cl:1][C:2]([Cl:9])([Cl:8])[CH:3]1[N:7]([C:10]([S-:12])=[S:11])[CH2:6][CH2:5][O:4]1.[Cl:1][C:2]([Cl:9])([Cl:8])[CH:3]1[N:7]([C:10]([S-:12])=[S:11])[CH2:6][CH2:5][O:4]1.[Zn+2:17]

참가 물질

6

실험 절차

95 2/10 g. of 2-trichloromethyloxazolidine (preparation described by W. Ruske and I. Hartmann, J. Prakt, Chem. 18, 146 (1962)) was dissolved in a mixture of 300 ml isopropanol, and 50.5 g. (0.50 mole) of carbon disulfide was added dropwise followed by 43.9 g. (0.25 mole) of anhydrous zinc acetate. The reaction mixture was heated for 2 hours at 45° - 50°C, cooled to room temperature, and diluted with 1 liter water; the precipitated product was filtered, washed thoroughly with water and dried in vacuo to give 86.3 g. of the crude product, melting at 193° - 195°C (decomp.). Hot benzene extractions of the crude product gave 38 g. of the desired carbodithioate sintering at 208°C, and melting 213° - 216°C (decomp.). It had the following analysis:

후처리

  1. temperatureThe reaction mixture was heated for 2 hours at 45° - 50°C
  2. filtrationthe precipitated product was filtered
  3. washwashed thoroughly with water
  4. customdried in vacuo
  5. customto give 86.3 g
  6. extractionHot benzene extractions of the crude product
  7. customgave 38 g
  8. customsintering at 208°C

출처 및 근거

ORD 기록
ord-e7c69df9ef1e4be2b9d6f130b850c0fc
출처 데이터셋
uspto-grants-1976_08
특허 번호
US03976648

연결된 노트

불러오는 중…