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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902002Generated: October 28, 2026

Water → 3-(3-Bromopropoxy-4-methoxyphenyl)phenylmethanone

https://huagongshe.com/reaction/1902002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
Reactant1,3-DibromopropaneHCID 8001—
ReactantSodium hydrideHCID 24758—
Reactant3-Hydroxy-4-methoxybenzophenoneHCID 4148893—
Product3-(3-Bromopropoxy-4-methoxyphenyl)phenylmethanoneHCID 21960089—

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 3-hydroxy-4-methoxybenzophenone (4.6 g, 20 mmol) in dimethylformamide (35 ml) was treated with sodium hydride (600 mg, 25 mmol) at 0° C. for 20 minutes, then 1,3-dibromopropane (5 g, 24.7 mmol) was added in one portion. The mixture was heated at 90° C. for 1 hour, and then stirred at room temperature for 2 hours. At the end of the reaction, the mixture was poured into water (500 ml) and extracted with ethyl acetate (400 ml). The ethyl acetate solution was washed with water, brine and dried over anhydrous MgSO4. The solvent was removed and the crude oil was purified by flash chromatography over a silica gel column (SiO2, 85 g; eluted with 3:1 hexane:dichloromethane, 1.6 1; 3:7 hexane: dichloromethane, 1.4 l). The pure product thus obtained weighed 4.67 g, (66%) as an oil. Recrystallization twice from isopropyl ether (500 ml) gave analytically pure 3-(3-bromopropoxy-4-methoxyphenyl) phenylmethanone (2.42 g), m.p.=81°-83° C.:.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578624
Source datasetuspto-grants-1996_11
ORD IDord-93bb7c7f691f4f3aa43f33e961c6d81e
Source noteuspto-grants-1996_11