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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22359Generated: October 25, 2026

3-Chloro-1-propanol → 2,3-dihydro-8-(3-hydroxypropoxy)-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-one

https://huagongshe.com/reaction/22359

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-1-propanolHCID 12313—
ReactantPotassium BicarbonateHCID 516893—
Reactant2,3-dihydro-8-hydroxy-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-oneHCID 19927677—
SolventIsopropanolHCID 3776—
Product2,3-dihydro-8-(3-hydroxypropoxy)-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-oneHCID 1992764858%

Reaction Steps

Method J (but using potassium hydrogencarbonate); Starting materials: 2,3-dihydro-8-hydroxy-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-one (example 109) and 3-chloro-1-propanol; yield 58%; fusion point 213°-215° C. (from isopropanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428038
Source datasetuspto-grants-1995_06
ORD IDord-ce7b2c4cccf04c1c9483a6157345c6e0
Source noteuspto-grants-1995_06