Phenacyl bromide → alpha-(3,4-Methylenedioxyphenoxy)acetophenone

HRID 46624

반응식

HRID 46624 반응식
[CH2:1]1[O:9][C:8]2[CH:7]=[CH:6][C:5]([OH:10])=[CH:4][C:3]=2[O:2]1.Br[CH2:12][C:13]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[O:14].C(=O)([O-])[O-].[Na+].[Na+].C(=O)([O-])[O-].[K+].[K+]>C1C=CC=CC=1>[CH2:1]1[O:9][C:8]2[CH:7]=[CH:6][C:5]([O:10][CH2:12][C:13]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)=[O:14])=[CH:4][C:3]=2[O:2]1

참가 물질

6

실험 절차

A mixture of 25 g. (0.181 mole) of 3,4-methylenedioxyphenol, 36 g. (0.181 mole) of α-bromoacetophenone and 41.2 g. (0.40 mole) of sodium carbonate in 350 ml. of benzene is heated to its reflux temperature and maintained at reflux for 16 hours. To the mixture is added 50 g. of potassium carbonate, and the mixture is refluxed for an additional 7 days while collecting water in a Barrett water trap. The mixture is then diluted with a mixture of water and benzene. The benzene layer is washed with water, then cold 5 percent sodium hydroxide solution. A precipitate forms in the benzene layer. It is collected, rinsed with benzene and dried to provide a white powder which is recrystallized from ethanol to provide α-(3,4-methylenedioxyphenoxy)acetophenone, m.p. 123°-126° C.

후처리

  1. additionA mixture of 25 g
  2. temperaturereflux temperature
  3. temperaturemaintained
  4. temperatureat reflux for 16 hours
  5. additionTo the mixture is added 50 g
  6. customwhile collecting water in a Barrett water trap
  7. additionThe mixture is then diluted with a mixture of water and benzene
  8. washThe benzene layer is washed with water
  9. customIt is collected
  10. washrinsed with benzene
  11. customdried
  12. customto provide a white powder which
  13. customis recrystallized from ethanol

출처 및 근거

ORD 기록
ord-b0a8a49ae46944b3a2df9093aa91678e
출처 데이터셋
uspto-grants-1979_11
특허 번호
US04174403

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