Morpholine → 5,5-Dichloro-1-morpholinopent-4-ene-1,3-dione

HRID 1765037

반응식

HRID 1765037 반응식
Cl[C:2]1([CH2:7][C:8]([Cl:11])([Cl:10])Cl)[O:5][C:4](=[O:6])[CH2:3]1.[NH:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1.C([O-])(O)=O.[Na+]>ClCCl.COC(C)(C)C>[Cl:11][C:8]([Cl:10])=[CH:7][C:2](=[O:5])[CH2:3][C:4]([N:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1)=[O:6]

참가 물질

6

반응 조건

온도
15 °C

실험 절차

Two separate solutions of 4-Chloro-4-(2,2,2-trichloro-ethyl)-oxetan-2-one (62.5 g, 0.26 mmol) and morpholine (24.0 g, 0.28 mol) in dichloromethane (120 ml) were added simultaneously to a mixture of NaHCO3 (44.0 g, 0.52 mol) in dry dichloromethane (300 ml). The reaction was maintained at 15° C. over 140 min with stirring. The reaction was filtered, washed with dichloromethane (3×100 ml) and the combined organic layers were concentrated in vacuo to a slurry which was then passed through a short silica pad, and further washed with dichloromethane (4×100 ml). The combined organic layers were concentrated in vacuo, suspended in hexane (400 ml) and stirred for 1 h, filtered and dried to give a cream solid. The solid was suspended in tert-butyl methyl ether (100 ml), stirred for 15 min, filtered, washed with butyl methyl ether and dried to give the desired compound as a white powder (47.8 g, 72%). m/z (LC-MS, ESP): 252 (M++1).

후처리

  1. filtrationThe reaction was filtered
  2. washwashed with dichloromethane (3×100 ml)
  3. concentrationthe combined organic layers were concentrated in vacuo to a slurry which
  4. washfurther washed with dichloromethane (4×100 ml)
  5. concentrationThe combined organic layers were concentrated in vacuo
  6. stirringstirred for 1 h
  7. filtrationfiltered
  8. customdried
  9. customto give a cream solid
  10. stirringstirred for 15 min
  11. filtrationfiltered
  12. washwashed with butyl methyl ether
  13. customdried

출처 및 근거

ORD 기록
ord-176d1684d67c4369a0dacaacdf0116ff
출처 데이터셋
uspto-grants-2007_06
특허 번호
US07226918B2

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