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1-(Triphenylphosphoranylidene)acetone → 1-(N-Cbz-2-pyrrolidinyl)-1-buten-3-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-(Triphenylphosphoranylidene)acetone | HCID 15038 | — |
| 反応物 | (S)-2-Formyl-pyrrolidine-1-carboxylic acid benzyl ester | HCID 11746545 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 1-(N-Cbz-2-pyrrolidinyl)-1-buten-3-one | HCID 57270246 | 69% |
反応手順
To a stirred solution of N-Cbz-L-prolinal (6.3 g, 27 mmol, from step 24d above) in 30 mL of benzene was added 9.42 g (29.6 mmol) of 1-triphenylphosphoranylidene-2-propanone (Aldrich) at room temperature. The reaction mixture was heated to reflux for 4 hr. The benzene was removed under vacuum, and the residue was dissolved in ether and cooled for 16 hr. The phosphine oxide by product was removed by filtration, and the solution was further purified by column chromatography on silica gel, eluting with 20% ethyl acetate in hexanes, to afford 4.4 g of the title product (69% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05424444 |
| 出典データセット | uspto-grants-1995_06 |
| ORD ID | ord-c84de9e588624ca4ad086efc5f1da219 |
| 出典メモ | uspto-grants-1995_06 |