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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Tetra-n-butylammonium tribromide | HCID 23500184 | — |
| Reactant | 1-(2-Phenoxypyrimidin-5-yl)ethanone | HCID 59252440 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-1-(2-phenoxypyrimidin-5-yl)ethanone | HCID 59252426 | 68.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08536185B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-394bb218ce9a406696585bd4e93d8732 |
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| Source note | uspto-grants-2013_09 |
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