HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (6-Oxopiperidin-2-yl)methyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 6-(Hydroxymethyl)piperidin-2-one | HCID 14506313 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (6-Oxopiperidin-2-yl)methyl methanesulfonate | HCID 90404452 | — |
Reaction Steps
6-(Hydroxymethyl)piperidin-2-one (1.0 g, 7.8 mmol) and Et3N (1.1 ml, 7.8 mmol) in DCM (5 ml) was added into mesyl chloride (0.88 g, 7.8 mmol) in DCM (20 ml) at 0° C. The reaction mixture was stirred at room temperature for 15 mins. The reaction mixture was washed with 1 N HCl (20 ml) and brine (40 ml), dried over anhydrous Na2SO4 and concentrated under reduced pressure to give (6-oxopiperidin-2-yl)methyl methanesulfonate which was used in the next step without additional purification. Yield (quant.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09133154B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-d7b04cd1ce0e4bb3a353ab45b4e6d790 |
| Source note | uspto-grants-2015_09 |