Piperidine → HCID 54536072、化合物
反応式
[O:1]=[C:2]1[CH2:11][CH2:10][CH2:9][C:8]2[CH:7]=[C:6]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH:5]=[CH:4][C:3]1=2.[N:17]1[CH:22]=[CH:21][CH:20]=[C:19]([CH:23]=O)[CH:18]=1.N1CCCCC1>C(O)(=O)C>[N:17]1[CH:22]=[CH:21][CH:20]=[C:19]([CH:23]=[C:11]2[CH2:10][CH2:9][C:8]3[CH:7]=[C:6]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH:5]=[CH:4][C:3]=3[C:2]2=[O:1])[CH:18]=1参加物
反応条件
- 温度
- 100 °C
実験手順
5.0 g of ethyl 5-oxo-5,6,7,8-tetrahydro-2-naphthalenecarboxylate was mixed with 2.5 g of 3-pyridinealdehyde, 10 ml of acetic acid and 10 ml of piperidine and then the mixture was stirred at 100° C. for 4 hours. The reaction mixture was concentrated in vacuo and the residue was dissolved in ethyl acetate. 10% Hydrochloric acid was added to the solution. The aqueous layer was separated and neutralized by addition of sodium bicarbonate. The mixture was extracted with chloroform. The extract was washed with water, dried and then concentrated in vacuo. The residue was purified by silica gel column chromatography to give 5.6 g of ethyl 6-(3-pyridylmethylidene)-5-oxo-5,6,7,8-tetrahydro-2-naphthalenecarboxylate as pale yellow crystals with m.p. 112°-114° C.
後処理
- concentrationThe reaction mixture was concentrated in vacuo
- dissolutionthe residue was dissolved in ethyl acetate
- addition10% Hydrochloric acid was added to the solution
- customThe aqueous layer was separated
- additionneutralized by addition of sodium bicarbonate
- extractionThe mixture was extracted with chloroform
- washThe extract was washed with water
- customdried
- concentrationconcentrated in vacuo
- customThe residue was purified by silica gel column chromatography
出典と根拠
- ORDレコード
- ord-92719ea9d3784d19a7fbd9a323175854
- 出典データセット
- uspto-grants-1988_10
- 特許番号
- US04777257
反応ノート
読み込み中…