Hydrochloric Acid → HCID 20406152, 화합물

HRID 2164304노트

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HRID 2164304 반응식
Br[C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][CH:3]=1.[Mg].[CH3:10][C:11]1[O:16][C:15](=[O:17])[C:14]2[CH:18]=[C:19]([CH3:22])[CH:20]=[CH:21][C:13]=2[N:12]=1.Cl>C(OCC)C.C1C=CC=CC=1>[F:8][C:5]1[CH:6]=[CH:7][C:2]([C:15]([C:14]2[CH:18]=[C:19]([CH3:22])[CH:20]=[CH:21][C:13]=2[NH:12][C:11](=[O:16])[CH3:10])=[O:17])=[CH:3][CH:4]=1

참가 물질

7

실험 절차

A Grignard reagent prepared from 87.5 g (0.5 mole) of p-bromofluorobenzene and excess magnesium in 800 ml of diethyl ether was slowly added to a solution of 2,6-dimethyl-3,1-benzoxazine-4-one in 300 ml of dry benzene and 200 ml of dry diethyl ether at 0° C. The mixture was allowed to warm to room temperature and stirring was continued for 2 hr. The reaction mixture was cooled to -15° C. and 500 ml of 3N hydrochloric acid was added. After about 10 min additional stirring, the organic layer was separated and washed with dilute sodium hydroxide solution. The organic layer was concentrated and the residue was dissolved in a mixture of 600 ml of 95% ethanol and 300 ml of 6N hydrochloric acid. The precipitate (crude titled product) in the amount of 123 g (ca 91%) was recrystallized from cyclohexane to give tan crystals, m.p. 140°-145° C.

후처리

  1. temperatureThe reaction mixture was cooled to -15° C.
  2. waitAfter about 10 min additional stirring
  3. customthe organic layer was separated
  4. washwashed with dilute sodium hydroxide solution
  5. concentrationThe organic layer was concentrated
  6. dissolutionthe residue was dissolved in a mixture of 600 ml of 95% ethanol and 300 ml of 6N hydrochloric acid
  7. customThe precipitate (crude titled product) in the amount of 123 g (ca 91%) was recrystallized from cyclohexane
  8. customto give tan crystals, m.p. 140°-145° C.

출처 및 근거

ORD 기록
ord-4282fddac26845a3aec9b860de65f6b3
출처 데이터셋
uspto-grants-1985_03
특허 번호
US04503073

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