Hydrochloric Acid → Spiro[indene-1,4'-piperidine] hydrochloride
反応式
C(OC([N:8]1[CH2:13][CH2:12][C:11]2([C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH:15]=[CH:14]2)[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:22]>C(OCC)(=O)C>[ClH:22].[NH:8]1[CH2:13][CH2:12][C:11]2([C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH:15]=[CH:14]2)[CH2:10][CH2:9]1参加物
4
実験手順
A solution of 1'-(tert-butyloxycarbonyl)spiro [indene-1,4'-piperidine] (3.0 g, 0.011 mol) in ethyl acetate (150 ml) was stirred at 0° C., and treated with hydrogen chloride for 30 minutes. The mixture was then evaporated to dryness, ethyl acetate (100 ml) was added, then removed in vacuo three times. The residue was stirred with anhydrous ether (200 ml), and the solid filtered off, to give spiro[indene-1,4'-piperidine] hydrochloride (2.3 g, 99%) as a pale yellow solid. The product was not purified further.
後処理
- customThe mixture was then evaporated to dryness, ethyl acetate (100 ml)
- additionwas added
- customremoved in vacuo three times
- filtrationthe solid filtered off
出典と根拠
- ORDレコード
- ord-ad79964c21e64bd3b773478810b12fed
- 出典データセット
- uspto-grants-1994_06
- 特許番号
- US05324733
反応ノート
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