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Methanesulfonyl chloride → 4-Benzoyl-1-methanesulphonylpiperidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methanesulfonyl chloride | HCID 31297 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 4-Benzoylpiperidine hydrochloride | HCID 2724437 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-Benzoyl-1-methanesulphonylpiperidine | HCID 16043536 | — |
反応手順
Neat DIPEA (1.54 ml, 8.86 mmol) was added dropwise to a solution of phenyl(4-piperidinyl)methanone hydrochloride (1 g, 4.43 mmol) in CH2Cl2 (20 ml) at 0° C. Then, neat MsCl (377 μL, 4.87 mmol) was slowly added and the cooling bath was removed. After 30 minutes, the reaction was quenched with water and diluted with CH2Cl2. After separation, the organic phase was washed with brine, dried over MgSO4 and evaporated to dryness. The final ketone 1 was obtained as a white solid (1.16 g, 98%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07361668B2 |
| 出典データセット | uspto-grants-2008_04 |
| ORD ID | ord-aa78a692c2cb4f939b8c603d3c78b629 |
| 出典メモ | uspto-grants-2008_04 |