참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 3-Methylpyridine | HCID 7970 | — |
| 반응물 | Methyl 2,3-dihydro-1H-indene-5-carboxylate | HCID 10464836 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Diisopropylamine | HCID 7912 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-(5-Indanyl)-2-(3-pyridyl)ethanone | HCID 13714653 | 83.2% |
반응 단계
In 80 ml of anhydrous tetrahydrofuran was dissolved 8.86 ml of diisopropylamine. The solution was cooled to -10°, to which was added dropwise 39.5 ml of a hexanoic solution of n-butyl lithium (1.6M). Then, the mixture was stirred for 30 minutes at the same temperature, followed by dropwise addition of 5.34 g of β-picoline. The mixture was stirred for 30 minutes, to which was added dropwise 5 g of 5-methoxycarbonyl indane dissolved in 10 ml of anhydrous tetrohydrofuran. Then, the mixture was stirred for one hour at room temperature, followed by addition of about 25 ml of water. The organic solvent was exaporated off under reduced pressure. The concentrated solution was subjected to extraction with ethylacetate. The extract solution was washed with water, dried on magnesium sulfate and concentrated. The concentrate was crystallized from ethylacetate-isopropylether to give 5.6 g (yield 82%) of 1-(5-indanyl)-2-(3-pyridyl)-ethanone, m.p. 55°-56° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04612321 |
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| 출처 데이터셋 | uspto-grants-1986_09 |
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| ORD ID | ord-4cc8ef99277c47c68418628848b35db2 |
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| 출처 메모 | uspto-grants-1986_09 |
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