참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phosphonium, (bromomethyl)triphenyl-, bromide (1:1) | HCID 2733422 | — |
| 반응물 | 6-Fluoroquinoline-2-carbaldehyde | HCID 3159605 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (Z)-2-(2-bromovinyl)-6-fluoroquinoline | HCID 86683113 | 65.4% |
반응 단계
To as suspension of (bromomethyl)triphenylphosphonium bromide (14.94 g, 34.3 mmol) in 100 mL of THF was added potassium tert-butoxide (3.84 g, 34.3 mmol) portionwise under Ar. Then the reaction mixture was stirred for 1 h at this temperature. 6-Fluoroquinoline-2-carbaldehyde (5 g, 28.5 mmol) in 40 mL of THF was added. The resulting reaction mixture was stirred for 5 h at −75° C. and allowed to warm up overnight. The reaction mixture was diluted with petrol ether and the solid was sucked off. The mother liquid was concentrated, diisopropyl ether was added and the formed precipitate was sucked off. The mother liquid was purified by column chromatography (cyclohexane/EA) to give 4.7 g (65.3%) of the title compound as brown solid. LC-MS: m/e 254.0.
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-20c5ec6bafca4fb0a9ce6892d8c2c734 |
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| 출처 메모 | uspto-grants-2016_03 |
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