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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042615Generated: November 3, 2026

1-Bromo-3-chloropropane → HCID 59651882, compound

https://huagongshe.com/reaction/2042615

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-Hydroxyphenyl)-3-methyl-4-oxo-butyric acid ethyl esterHCID 59651952—
SolventAcetoneHCID 180—
ProductHCID 59651882HCID 5965188258.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 4-(4-hydroxyphenyl)-3-methyl-4-oxo-butyric acid ethyl ester (12.5 g, 52.9 mmol), 1-bromo-3-chloropropane (11.3 mL, 114.6 mmol) and K2CO3 (21.9 g, 159 mmol) in acetone (200 mL) was stirred at 60° C. for 15 h. The reaction was cooled to RT and filtered over celite and the filtrate was evaporated at reduced pressure to give a crude residue. The crude residue was partitioned between methylene chloride and saturated aqueous sodium bicarbonate solution and the aqueous layer was extracted twice with methylene chloride. The combined organics was washed with brine, dried (Na2SO4), filtered, and concentrated to provide a crude product. The crude product was purified by ISCO (330 g) chromatography using 15% EtOAc in hexane to produce 4-[4-(3-chloro-propoxy)-phenyl]-3-methyl-4-oxo-butyric acid ethyl ester (9.7 g, 56%), MS m/z 267 (M−45)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586588B2
Source datasetuspto-grants-2013_11
ORD IDord-e4c835008b5d4674a9a8d9d80b44a88e
Source noteuspto-grants-2013_11