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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42300Generated: October 25, 2026

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

https://huagongshe.com/reaction/42300

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 numberUS08536185B2
Source datasetuspto-grants-2013_09
ORD IDord-394bb218ce9a406696585bd4e93d8732
Source noteuspto-grants-2013_09