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3-Bromobenzaldehyde → 1-Bromo-3-(2-methyl-1-propenyl)benzene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Bromobenzaldehyde | HCID 76583 | — |
| 反応物 | Isopropyltriphenylphosphonium iodide | HCID 2723783 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 触媒 | 18-Crown-6 | HCID 28557 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1-Bromo-3-(2-methyl-1-propenyl)benzene | HCID 21706836 | 75.3% |
反応手順
To a stirred slurry of 17.83 g (41.2 mmol) of isopropyltriphenylphosphonium iodide and 300 mg (1.1 mmol) of 18-crown-6 in 50 mL of THF under nitrogen at 5° C. was added 4.60 g (41.0 mmol) of potassium t-butoxide over 5 minutes. The resulting deep red-orange slurry was stirred 10 minutes and then a solution of 4.31 mL (37.0 mmol) of 3-bromobenzaldehyde in 40 mL of THF was added at a rate to keep the temperature below 10° C. The resulting bright yellow slurry was stirred for 20 minutes and then poured into 300 mL of hexanes. The solids were filtered off and the filtrate evaporated. This residue was purified by flash chromatography (5×15 cm column) and eluted with hexanes to provide 5.88 g (75%) of title compound as a colorless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05157027 |
| 出典データセット | uspto-grants-1992_10 |
| ORD ID | ord-2e4bd4a7bf1b4401a81feba32fb102f2 |
| 出典メモ | uspto-grants-1992_10 |