Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3767Generated: October 28, 2026

Piperidine → 6-Methoxy-4-piperidino-2,3-dihydrobenzopyran

https://huagongshe.com/reaction/3767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 13712845HCID 13712845—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product6-Methoxy-4-piperidino-2,3-dihydrobenzopyranHCID 13712846—

Reaction Steps

Methane sulfonyl chloride (14.9 ml) is added dropwise to a stirred solution of the product obtained in Step 1. (31.6 g) and triethylamine (29.3 ml) in methylene chloride (750 ml) cooled to 0° C. under nitrogen. The reaction mixture is stirred at RT for 21/2 hours and cooled to 0° C. Piperidine (175 ml) is added to the cooled reaction mixture and the solution stirred at RT overnight. Sat'd aq. sodium bicarbonate is added to the solution and the mixture is stirred for 30 minutes. The organic layer is separated, washed with sat'd NaCl and dried. The solution is filtered and the filtrate evaporated in vacuo yielding the desired product as its hydrochloride salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04722925
Source datasetuspto-grants-1988_02
ORD IDord-649ea945dd7e4b54ae14924d504966d6
Source noteuspto-grants-1988_02