1,1-Bis(methylthio)-2-nitroethylene → HCID 70537224, 화합물

HRID 1277996노트

반응식

HRID 1277996 반응식
[CH3:1][S:2][C:3](SC)=[CH:4][N+:5]([O-:7])=[O:6].[NH2:10][CH2:11][CH2:12][CH2:13][O:14][CH2:15][C:16]1[O:20][C:19]([CH2:21][N:22]([CH3:24])[CH3:23])=[CH:18][CH:17]=1>O1CCOCC1>[CH3:24][N:22]([CH3:23])[CH2:21][C:19]1[O:20][C:16]([CH2:15][O:14][CH2:13][CH2:12][CH2:11][NH:10][C:3]([S:2][CH3:1])=[CH:4][N+:5]([O-:7])=[O:6])=[CH:17][CH:18]=1

참가 물질

4

실험 절차

To a stirred solution of 1,1-bis(methylthio)-2-nitroethene (3.96 g) in dry dioxan (25 ml) at 70° was added dropwise 5-[(3-aminopropoxy)methyl]-N,N-dimethyl-2-furanmethanamine (1.27 g). After 1 hr the reaction was allowed to cool and the solid which separated was filtered. The filtrate and washings were combined and evaporated to dryness, a solution of succinic acid (1 g) in water (25 ml) added to the residue and the suspension filtered. The filtrate was washed with ethyl acetate (2×40 ml) then evaporated to 10 ml. The solution was basified with sodium carbonate and the oily precipitate which separated was extracted into ethyl acetate (3×25 ml). The combined extracts were dried (anhyd. sodium carbonate), the suspension filtered and evaporated to dryness to yield the title compound (1.34 g) as a brown oil.

후처리

  1. temperatureto cool
  2. customthe solid which separated
  3. filtrationwas filtered
  4. customevaporated to dryness
  5. additiona solution of succinic acid (1 g) in water (25 ml) added to the residue
  6. filtrationthe suspension filtered
  7. washThe filtrate was washed with ethyl acetate (2×40 ml)
  8. customthen evaporated to 10 ml
  9. customthe oily precipitate which separated
  10. extractionwas extracted into ethyl acetate (3×25 ml)
  11. dry with materialThe combined extracts were dried (anhyd. sodium carbonate)
  12. filtrationthe suspension filtered
  13. customevaporated to dryness

출처 및 근거

ORD 기록
ord-9e2e890c13584e489ee91686fc7d8648
출처 데이터셋
uspto-grants-1981_07
특허 번호
US04279911

반응 노트

불러오는 중…