HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonyl chloride → Ethyl 1-(phenylsulfonyl)piperidine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl nipecotate | HCID 98969 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 1-(phenylsulfonyl)piperidine-3-carboxylate | HCID 2904534 | 94.6% |
Reaction Steps
A mixture of ethyl piperidine-3-carboxylate (1.00 g, 6.36 mmol), benzenesulfonyl chloride (0.812 mL, 6.36 mmol), and triethylamine (2.66 mL, 19.1 mmol) in methylene chloride (10.0 mL) was stirred at r.t. for 2 hours. The mixture was quenched with water, then extracted with ethyl acetate. The extract was washed with 1N HCl solution, water, sat'd sodium bicarbonate solution, water, and brine, successively. Then, the extract was dried over sodium sulfate (anhydrous). After filtration, the filtrate was concentrated to yield 1.79 g (94%) of ethyl 1-(phenylsulfonyl)piperidine-3-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071624B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-d165c8a71e7d4f48b27d35b029d9dec2 |
| Source note | uspto-grants-2011_12 |