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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859425Generated: November 1, 2026

Triethylamine → (R)-3-chloro-1-(3-methoxyphenethyl)homopiperidine

https://huagongshe.com/reaction/1859425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant(R)-2-Hydroxymethyl-1-(3-methoxyphenethyl)piperidineHCID 69900408—
SolventDichloromethaneHCID 6344—
Product(R)-3-chloro-1-(3-methoxyphenethyl)homopiperidineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528504B2
Source datasetuspto-grants-2003_03
ORD IDord-a59cb0c3e7844591a679b7eb3c31022f
Source noteuspto-grants-2003_03