Ethanol → Benzylsulfanylmethyl-5-cyclopropyl-imidazolidine-2,4-dione

HRID 1441502노트

반응식

HRID 1441502 반응식
[CH2:1]([S:8][CH2:9]C(C1CC1)=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C-]#N.[Na+].[C:18](=[O:21])([O-])[O-].[NH4+:22].[NH4+:23].[CH3:24][C:25](OC)([CH3:27])C.[CH2:30]([OH:32])[CH3:31]>O>[CH3:5][CH2:4][CH2:3][CH:2]([CH3:7])[CH3:1].[CH2:1]([S:8][CH2:9][N:22]1[CH:31]([CH:27]2[CH2:24][CH2:25]2)[C:30](=[O:32])[NH:23][C:18]1=[O:21])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

참가 물질

8

반응 조건

온도
90 °C

실험 절차

2-Benzylsulfanyl-1-cyclopropyl-ethanone (27.55 g, 0.133 mol) was dissolved in ethanol (250 ml) and dispensed into 20×40 ml vials. Sodium cyanide (6.52 g, 0.133 mol) and ammonium carbonate (64 g, 0.667 mol) were dissolved in water (250 ml) and divided into the vials, which were then sealed and heated at 90° C. for 5 h behind a safety screen. After cooling to room temperature, the contents of the vials were combined, TBME was added, and the mixture was washed with water (×2), brine (×1), and then dried over sodium sulphate. Evaporation then gave the crude product (16.5 g, 45%). This material was absorbed onto silica and chromatographed (5×9.5 cm column of silica) eluting with iso-hexane to 50% ethyl acetate:iso-hexane to yield the title compound (11.81 g, 32.1%).

후처리

  1. customwere then sealed
  2. temperatureAfter cooling to room temperature
  3. washthe mixture was washed with water (×2), brine (×1)
  4. dry with materialdried over sodium sulphate
  5. customEvaporation
  6. customthen gave the crude product (16.5 g, 45%)
  7. customThis material was absorbed onto silica
  8. customchromatographed (5×9.5 cm column of silica)
  9. washeluting with iso-hexane to 50% ethyl acetate

출처 및 근거

ORD 기록
ord-645ad512b6504166b683bdff146d5ff8
출처 데이터셋
uspto-grants-2010_02
특허 번호
US07655664B2

반응 노트

불러오는 중…