참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Sulfate | HCID 24436 | — |
| 반응물 | Hydride | HCID 166653 | — |
| 반응물 | Aluminium lithium hydride | HCID 21226445 | — |
| 반응물 | Spiro(cyclopentane-1,1'-indan)-3'-ylideneacetonitrile | HCID 54124997 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 3'-beta-Aminoethylidene-spiro(cyclopentane-1,1'-indan) | HCID 54082998 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04172093 |
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| 출처 데이터셋 | uspto-grants-1979_10 |
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| ORD ID | ord-16b0d6a7dd3a44aaa813ec73ce084db6 |
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| 출처 메모 | uspto-grants-1979_10 |
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