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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274492Generated: October 27, 2026

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

https://huagongshe.com/reaction/2274492

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)methanoneHCID 11799382871.3%

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 numberUS09126973B2
Source datasetuspto-grants-2015_09
ORD IDord-f5fcb93393f24e76ac5f731bef4530a1
Source noteuspto-grants-2015_09