Hydrochloric Acid → HCID 20406152、化合物
反応式
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]=1参加物
実験手順
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.
後処理
- temperatureThe reaction mixture was cooled to -15° C.
- waitAfter about 10 min additional stirring
- customthe organic layer was separated
- washwashed with dilute sodium hydroxide solution
- concentrationThe organic layer was concentrated
- dissolutionthe residue was dissolved in a mixture of 600 ml of 95% ethanol and 300 ml of 6N hydrochloric acid
- customThe precipitate (crude titled product) in the amount of 123 g (ca 91%) was recrystallized from cyclohexane
- customto give tan crystals, m.p. 140°-145° C.
出典と根拠
- ORDレコード
- ord-4282fddac26845a3aec9b860de65f6b3
- 出典データセット
- uspto-grants-1985_03
- 特許番号
- US04503073
反応ノート
読み込み中…