Piperidine → 2-(Pyridin-4-ylmethylidene)-3,4-dihydronaphthalen-1-one
반응식
[CH2:1]1[CH2:11][C:9](=[O:10])[C:8]2[C:3](=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH2:2]1.[N:12]1[CH:17]=[CH:16][C:15]([CH:18]=O)=[CH:14][CH:13]=1.N1CCCCC1>C(O)(=O)C>[N:12]1[CH:17]=[CH:16][C:15]([CH:18]=[C:11]2[CH2:1][CH2:2][C:3]3[C:8](=[CH:7][CH:6]=[CH:5][CH:4]=3)[C:9]2=[O:10])=[CH:14][CH:13]=1참가 물질
5
실험 절차
A mixture of 73.0 grams (0.50 moles) of α-tetralone, 64.2 grams (0.60 moles) of 4-pyridinecarboxaldehyde, 10 grams of piperidine and 10 grams of acetic acid are heated at 80° for 19 hours. The resultant solid is crystallized from about 400 ml. of ethanol to give 2-(4-pyridylmethylene)- 1-tetralone; (m.p. 112°-114°C).
후처리
- temperatureare heated at 80° for 19 hours
- customThe resultant solid is crystallized from about 400 ml
출처 및 근거
- ORD 기록
- ord-40b25525dc954f0f82aa11e588b440a5
- 출처 데이터셋
- uspto-grants-1976_01
- 특허 번호
- US03932430
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