HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867867Generated: October 27, 2026
Piperidine → 7-Methoxy-3-piperidino-2,2-dimethylbenzofuran
https://huagongshe.com/reaction/867867
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 7-Methoxy-3-hydroxy-2,2-dimethylbenzofuran | HCID 14126648 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 7-Methoxy-3-piperidino-2,2-dimethylbenzofuran | HCID 14126649 | — |
Reaction Steps
Triethylamine (29 ml) is added to a stirred solution of the product obtained in Step 4. (25.4 g) in methylene chloride (560 ml) at RT under nitrogen. Methanesulfonyl chloride (11.1 ml) is added dropwise to the mixture which is cooled to 0° C. The mixture is stirred for 3 hours at RT, cooled to 0° C., piperidine (128 ml) added and stirring continued at RT overnight. Sat'd aq. sodium bicarbonate is added to the mixture, the phases separated and the organic phase washed with sodium bicarbonate, sat'd NaCl, dried, filtered and evaporated in vacuo. The residue is dissolved in toluene and evaporated in vacuo affording the desired product as the hydrochloride salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04777168 |
|---|
| Source dataset | uspto-grants-1988_10 |
|---|
| ORD ID | ord-35781814d3f34c069d77d07574c984ab |
|---|
| Source note | uspto-grants-1988_10 |
|---|