Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867864Generated: October 25, 2026

1,3-Dibromopropane → 6-(3-Bromopropoxy)-4-piperidino-2,3-dihydrobenzopyran

https://huagongshe.com/reaction/867864

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromopropaneHCID 8001—
ReactantPotassium HydroxideHCID 14797—
Reactant6-Hydroxy-4-piperidino-2,3-dihydrobenzopyranHCID 13712848—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventDiethyl EtherHCID 3283—
Product6-(3-Bromopropoxy)-4-piperidino-2,3-dihydrobenzopyranHCID 13712849—

Reaction Steps

Crushed potassium hydroxide (1.15 g) and tetrabutyl ammonium chloride (0.61 g) are added to a solution of the product obtained in Step 3. (4.8 g) in 1,3-dibromopropane (21 ml). The reaction mixture is stirred under nitrogen at RT for 48 hours, diluted with diethyl ether, washed with water and extracted into 5% aq. HCl. The aqueous solution is washed with ether and made alkaline yielding a yellow oil which is taken up in ether, washed, dried, filtered and evaporated to give the desired product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04777168
Source datasetuspto-grants-1988_10
ORD IDord-95b8a8006132494983a856a17648bc51
Source noteuspto-grants-1988_10