반응식
[O:1]=[C:2]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[O:5][CH:4]=[C:3]1[CH:12]=O.Cl.[NH2:15]O.C([O-])=O.[Na+].C(O)=O>O>[O:1]=[C:2]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[O:5][CH:4]=[C:3]1[C:12]#[N:15]참가 물질
6
실험 절차
A mixture of 26.1 g. (0.15 mole) of 4-oxo-4H-1-benzopyran-3-carboxaldehyde, 13.1 g. (0.19 mole) of hydroxylamine hydrochloride, 18.4 g. (0.27 mole) of sodium formate and 250 ml of 99% formic acid was heated with stirring at reflux for 21/2 hours. Water was added to 1-liter volume. The separated solid was filtered from the cooled mixture, washed well with water and dried to give 13 g. (51%) of crude nitrile melting at 138°-145°C. Recrystallization from ethylacetate gave pure, white crystals melting at 174°-176°.
후처리
- additionA mixture of 26.1 g
- temperatureat reflux for 21/2 hours
- filtrationThe separated solid was filtered from the cooled mixture
- washwashed well with water
- customdried
- customto give 13 g
- customRecrystallization from ethylacetate
- customgave pure
출처 및 근거
- ORD 기록
- ord-374965f0f83b449f936ea6acdee65858
- 출처 데이터셋
- uspto-grants-1976_02
- 특허 번호
- US03937837
연결된 노트
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