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1,2-Dichloroethane → 2-(2-Fluorophenyl)-1-(piperidin-4-yl)ethanone hydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,2-Dichloroethane | HCID 11 | — |
| 反応物 | 1-(1-Benzylpiperidin-4-yl)-2-(2-fluorophenyl)ethanone | HCID 22247993 | — |
| 溶媒 | 1-Chloroethyl chloroformate | HCID 521305 | — |
| 生成物 | 2-(2-Fluorophenyl)-1-(piperidin-4-yl)ethanone hydrochloride | HCID 22248124 | 92% |
反応手順
After dissolving 1.27 g of 1-(1-benzylpiperidin-4-yl)-2-(2-fluorophenyl)ethanone in 8 ml of 1,2-dichloroethane, 0.53 ml of 1-chloroethyl chloroformate was added while stirring on ice, and the mixture was heated to reflux for 1 hour. The solvent was distilled off under reduced pressure, 8 ml of methanol was added to the residue, and heating to reflux was continued for 40 minutes. The solvent was distilled off under reduced pressure, ethyl acetate was added to the residue, and the precipitate was filtered out to obtain the title compound (970 mg, 92% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07265108B2 |
| 出典データセット | uspto-grants-2007_09 |
| ORD ID | ord-73d21e929b3845a39e8174d64c041f64 |
| 出典メモ | uspto-grants-2007_09 |