HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (R)-3-chloro-1-(3-methoxyphenethyl)homopiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (R)-2-Hydroxymethyl-1-(3-methoxyphenethyl)piperidine | HCID 69900408 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-3-chloro-1-(3-methoxyphenethyl)homopiperidine | HCID 22975049 | — |
Reaction Steps
(R)-2-Hydroxymethyl-1-(3-methoxyphenethyl)piperidine (322 mg, 1.28 mmol) was dissolved in 10 ml of dichloromethane. Triethylamine (170 mg, 1.68 mmol) and methanesulfonyl chloride (192 mg, 1.68 mmol) were added to the obtained solution under stirring under cooling on ice. They were stirred under cooling on ice for 1 hour and then at room temperature for 18 hours. The reaction liquid was distributed in dichloromethane and saturated aqueous sodium hydrogencarbonate solution. The organic layer was dried over magnesium sulfate, and the solvent was evaporated under reduced pressure to obtain (R)-3-chloro-1-(3-methoxyphenethyl)homopiperidine in the form of a light yellow oil (182 mg, 53%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06528504B2 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-a59cb0c3e7844591a679b7eb3c31022f |
| Source note | uspto-grants-2003_03 |