반응식
[C:1]12([CH2:16][CH2:15][CH2:14][CH2:13]1)[C:9]1[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=1)[C:3](=[CH:10][C:11]#[N:12])[CH2:2]2.[H-].[Al+3].[Li+].[H-].[H-].[H-].[H-].S([O-])([O-])(=O)=O.[Na+].[Na+]>CCOCC>[NH2:12][CH2:11][CH:10]=[C:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[C:1]2([CH2:16][CH2:15][CH2:14][CH2:13]2)[CH2:2]1참가 물질
실험 절차
A solution of spiro(cyclopentane-1,1'-indan)-3'-ylideneacetonitrile (10.5 g; 0.05 moles) in anhydrous ether (100 ml) is added dropwise under agitation to lithium aluminum hydride (2.5 g; 0.066 moles) suspended in ether (200 ml). After boiling for 3 hours the mixture is cooled to room temperature and the excess of hydride is decomposed by dropwise addition of a saturated sodium sulphate solution. The precipitate obtained is filtered off and washed with ether. The ether solutions are shaken with 2 N hydrochloric acid. The acid extracts are concentrated to a small volume in vacuum (bath temperature below 40° C.) and the amine hydrochloride is precipitated by treatment with conc. hydrochloric acid in the cooled. Yield 10.6 g (85%). Recrystallization from 2-propanol yields colourless crystals of mp. 190° C. identical with the product prepared according to example 3g.
후처리
- customThe precipitate obtained
- filtrationis filtered off
- washwashed with ether
- concentrationThe acid extracts are concentrated to a small volume in vacuum (bath temperature below 40° C.)
- customthe amine hydrochloride is precipitated by treatment with conc. hydrochloric acid in the cooled
- customRecrystallization from 2-propanol
- customyields colourless crystals of mp. 190° C. identical with the product
- customprepared
출처 및 근거
- ORD 기록
- ord-16b0d6a7dd3a44aaa813ec73ce084db6
- 출처 데이터셋
- uspto-grants-1979_10
- 특허 번호
- US04172093
연결된 노트
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