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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456786Generated: October 30, 2026

Acetone → 1-[4-(3-Chloropropoxy)-2-hydroxy-5-methoxyphenyl]ethanone

https://huagongshe.com/reaction/1456786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(2,4-Dihydroxy-5-methoxyphenyl)ethan-1-oneHCID 49850540—
SolventWaterHCID 962—
Product1-[4-(3-Chloropropoxy)-2-hydroxy-5-methoxyphenyl]ethanoneHCID 1846724370.3%

Reaction Steps

A mixture of 2,4-dihydroxy-5-methoxyacetophenone (1.4 g, 7.7 mmol), K2CO3 (1.4 g, 10.0 mmol), 3-chlorobromopropane (1.6 g, 10.0 mmol) and acetone (25 mL) was stirred and refluxed under N2 for 16 hours. The reaction was poured into H2O, and the aqueous suspension was extracted with ethyl acetate. The extract was washed (H2O, brine) dried (MgSO4) and concentrated to yield 1.4 g of an off-white solid. Recrystallization twice from ethanol afforded 0.4 g of the alkylated phenol as a solid, m.p. 99°-101° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843977
Source datasetuspto-grants-1998_12
ORD IDord-5bbb3275b1cb45f39c0d3e6ae7dd379f
Source noteuspto-grants-1998_12