HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216980Generated: October 31, 2026
Phosphorus oxybromide → HCID 21946020, compound
https://huagongshe.com/reaction/2216980
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxybromide | HCID 24613 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 21946010 | HCID 21946010 | — |
| Solvent | Dibromomethane | HCID 3024 | — |
| Product | HCID 21946020 | HCID 21946020 | — |
Reaction Steps
(±)-1-(2,4-Dichloro-pyrimidin-5-yl)-2-methyl-propan-1-ol (0.18 g; 0.83 mmol) (from Example 11a supra) was combined with N,N-diisopropyl-ethylamine (0.37 mL; 2.10 mmol) (Aldrich) and a small volume of dibromomethane (50 μL) (Aldrich) to help solubilize the mixture. Only a small amount of material remained insoluble. Neat phosphorus oxybromide (0.22 g; 0.85 mmol) (Aldrich) was added in one portion. Reaction mixture was stirred for 10 minutes and then partitioned between ethyl acetate and water. The organic phase was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated. Purification by flash chromatography (Biotage 12M) gave (±)-5-(1-bromo-2-methyl-propyl)-2,4-dichloro-pyrimidine as a colorless oil. (Yield 79.5 mg; 33.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07112676B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-0065ed9206114f5cba91504e52eba4df |
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| Source note | uspto-grants-2006_09 |
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