참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Quinolinecarboxaldehyde | HCID 79619 | — |
| 반응물 | Phosphonium, (bromomethyl)triphenyl-, bromide (1:1) | HCID 2733422 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (Z)-2-(2-Bromovinyl)quinoline | HCID 15364160 | 59.1% |
반응 단계
A suspension of 24.97 g (57.3 mmol) of (bromomethyl)triphenylphosphonium bromide in 160 mL of THF was chilled to −70° C. under argon. Then, 6.43 g (57.3 mmol) of potassium tert-butoxide were added portionwise and the suspension was allowed to stir at this temperature for 1 h. A solution of 7.5 g of (47.7 mmol) quinoline-2-carbaldehyde in 40 mL of THF was slowly added dropwise. The mixture was allowed to stir at −75° C. for further 5 hours and then warmed to room temperature overnight. 160 mL of PE were added. The precipitate formed was sucked off. The mother liquid was evaporated and the residue was stirred with diisopropyl ether. The residue formed was sucked off. Purification by chromatography (heptane/EA 3/1) yielded 6.6 g (59.1%) of the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09273068B2 |
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| 출처 데이터셋 | uspto-grants-2016_03 |
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| ORD ID | ord-610107384e8d4a35a8698cd063865337 |
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| 출처 메모 | uspto-grants-2016_03 |
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