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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096334Generated: October 27, 2026

Hexane → 2-Bromo-1-(2-phenoxypyrimidin-5-yl)ethanone

https://huagongshe.com/reaction/2096334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantTetra-n-butylammonium tribromideHCID 23500184—
Reactant1-(2-Phenoxypyrimidin-5-yl)ethanoneHCID 59252440—
SolventDichloromethaneHCID 6344—
Product2-Bromo-1-(2-phenoxypyrimidin-5-yl)ethanoneHCID 5925242668.4%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution consisting of 1-(2-phenoxypyrimidin-5-yl)ethanone (Step B, 400 mg, 1.87 mmol) in dichloromethane (14 mL) was added tetrabutylammonium tribromide (990 mg, 2.05 mmol). The reaction mixture was sealed with a screw top and warmed at 40° C. overnight and allowed to cool to room temperature. Hexane (4 mL) was subsequently added. After three hours and little precipitation, additional (150 mg) tetrabutylammonium tribromide was added and the reaction mixture was stirred overnight at room temperature. The pale yellow precipitate that formed was collected on a filter and washed with 1:1 dichloromethane-hexane to afford the title intermediate (375 mg, 68%); Rf 0.43 with 3:1 v/v hexanes-ethyl acetate; MS (ESI+) m/z 295, 293 (M+1, Br isotopes).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450326B2
Source datasetuspto-grants-2013_05
ORD IDord-9d9742b2c26c4051a32727852575aaa1
Source noteuspto-grants-2013_05