HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → 4-Benzoyl-1-methanesulphonylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Benzoylpiperidine hydrochloride | HCID 2724437 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Benzoyl-1-methanesulphonylpiperidine | HCID 16043536 | — |
Reaction Steps
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%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07361668B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-aa78a692c2cb4f939b8c603d3c78b629 |
| Source note | uspto-grants-2008_04 |