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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799507Generated: October 25, 2026

Triethylamine → 1-Ethoxycarbonyl-4-methyloxypiperidine

https://huagongshe.com/reaction/1799507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantEthyl 4-hydroxypiperidine-1-carboxylateHCID 96394—
SolventEthyl AcetateHCID 8857—
Product1-Ethoxycarbonyl-4-methyloxypiperidineHCID 45120191—

Reaction Conditions

Temperature3 °C

Reaction Steps

1-ethoxycarbonyl-4-hydroxypiperidine (30.3 g) and triethylamine (23 g) were dissolved in ethyl acetate (182 mL) and the obtained mixture was cooled to 3° C. Methanesulfonyl chloride (22.05 g) was added thereto under stirring while taking caution such that the temperature did not exceed 20° C., and the mixture was continuously stirred under ice cooling for 1 hour. The obtained reaction mixture was washed with water (90 mL×3). The organic layer was isolated and concentrated to obtain a target compound as a light yellow oily substance. The yield amount was 43.09 g (98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344148B2
Source datasetuspto-grants-2013_01
ORD IDord-825ac70ecbe74447a4d3ae61ee06014d
Source noteuspto-grants-2013_01