Phosphorus sulfide (P2S5) → methyl 3,4-dihydro-2-isopropyl-3-thioxo-2H-1,4-benzoxazine-4-acetate
반응식
[CH:1]([CH:4]1[C:9](=O)[N:8]([CH2:11][C:12]([O:14][CH3:15])=[O:13])[C:7]2[CH:16]=[CH:17][CH:18]=[CH:19][C:6]=2[O:5]1)([CH3:3])[CH3:2].P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:21]>C1(C)C=CC=CC=1>[CH:1]([CH:4]1[C:9](=[S:21])[N:8]([CH2:11][C:12]([O:14][CH3:15])=[O:13])[C:7]2[CH:16]=[CH:17][CH:18]=[CH:19][C:6]=2[O:5]1)([CH3:3])[CH3:2]참가 물질
4
실험 절차
A mixture of methyl 3,4-dihydro-2-isopropyl-3-oxo-2H-1,4-benzoxazine-4-acetate (26.0 g), phosphorus pentasulfide (44.4 g) and toluene (250 ml) was refluxed for 3 hours with heating. After cooling the insoluble matter was removed by filtration, and the solvent was evaporated off. To the residue, isopropyl ether (200 ml) was added and the insoluble matter was removed by filtration. The solvent was evaporated off, and hexane was added to the residue, to give crystals of methyl 3,4-dihydro-2-isopropyl-3-thioxo-2H-1,4-benzoxazine-4-acetate. Yield was 22.5 g (80.6%). Recrystallization from isopropyl alcohol gave yellow prisms (mp 60°-61° C.).
후처리
- temperaturewas refluxed for 3 hours
- temperaturewith heating
- temperatureAfter cooling the insoluble matter
- customwas removed by filtration
- customthe solvent was evaporated off
- additionTo the residue, isopropyl ether (200 ml) was added
- customthe insoluble matter was removed by filtration
- customThe solvent was evaporated off
- additionhexane was added to the residue
출처 및 근거
- ORD 기록
- ord-d8c49f9c43b94e2780ab5045267c9c1f
- 출처 데이터셋
- uspto-grants-1988_09
- 특허 번호
- US04771050
반응 노트
불러오는 중…