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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684219Generated: November 4, 2026

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

https://huagongshe.com/reaction/1684219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant1-Bromo-3-chloropropaneHCID 8006—
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), K2O3 (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 numberUS05639764
Source datasetuspto-grants-1997_06
ORD IDord-72159bd0a85f40f88cf79d6ac37870ef
Source noteuspto-grants-1997_06