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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683612Generated: November 3, 2026

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

https://huagongshe.com/reaction/1683612

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 numberUS05637710
Source datasetuspto-grants-1997_06
ORD IDord-ad5ada3c5dc94920854a40e7a53dafa0
Source noteuspto-grants-1997_06