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tert-Butyl (triphenylphosphoranylidene) acetate → (E)t-Butyl 7-phenyl-2-heptenoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | tert-Butyl (triphenylphosphoranylidene) acetate | HCID 256127 | — |
| 反応物 | Benzenepentanal | HCID 561886 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (E)t-Butyl 7-phenyl-2-heptenoate | HCID 10659015 | 77.6% |
反応手順
A stirred solution of 5-phenylpentanal (9.96 g, Reference Example 6) in anhydrous tetrahydrofuran (100 ml) at room temperature was treated with (tert-butoxycarbonylmethylene)triphenylphosphorane (27.5 g). The resulting orange solution was stirred for 2.5 hours then evaporated. The residual crude product was subjected to flash chromatography on silica eluting with a mixture of hexane and ethyl acetate (19:1, v/v) to afford the title compound (12.4 g) as a colourless oil. NMR (CDCl3): δ1.45 (s,9H), 1.65 (m,4H), 2.18 (q,2H), 2.61 (t,2H), 5.70 (d,1H), 6.82 (dt,1H), 7.10-7.30 (m,5H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06306873B1 |
| 出典データセット | uspto-grants-2001_10 |
| ORD ID | ord-eba8236c74a9422e9aa2c48de5d45be3 |
| 出典メモ | uspto-grants-2001_10 |