反応式
S(O[CH2:12][CH2:13][CH:14]1[CH2:18][C:17]2[CH:19]=[CH:20][CH:21]=[CH:22][C:16]=2[O:15]1)(C1C=CC(C)=CC=1)(=O)=O.[OH:23][C:24]1([C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)[CH2:29][CH2:28][NH:27][CH2:26][CH2:25]1.C(=O)([O-])[O-].[Na+].[Na+]>CC(C)CC(=O)C>[OH:23][C:24]1([C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)[CH2:29][CH2:28][N:27]([CH2:12][CH2:13][CH:14]2[CH2:18][C:17]3[CH:19]=[CH:20][CH:21]=[CH:22][C:16]=3[O:15]2)[CH2:26][CH2:25]1参加物
5
実験手順
The mixture of 4.6 g of 2-(2-tosyloxyethyl)-2,3-dihydrobenzofuran, 2.64 g of 4-hydroxy-4-phenylpiperidine, 10 g of anhydrous sodium carbonate and 100 ml of 4-methyl-2-pentanone is relfuxed for 48 hours. It is filtered, evaporated and the residue recrystallized from isopropanol-petroleum ether, to yield the 2-[2-(4-hydroxy-4-phenylpiperidino)-ethyl]-2,3-dihydrobenzofuran melting at 107°.
後処理
- filtrationIt is filtered
- customevaporated
- customthe residue recrystallized from isopropanol-petroleum ether
出典と根拠
- ORDレコード
- ord-eaadb055c411437da796978a45fc7ac1
- 出典データセット
- uspto-grants-1977_08
- 特許番号
- US04039676
関連ノート
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