HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046103Generated: October 26, 2026
1-(5-Bromopyrimidin-2-yl)ethan-1-one → 2-(5-Bromopyrimidin-2-yl)propan-2-ol
https://huagongshe.com/reaction/1046103
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(5-Bromopyrimidin-2-yl)ethan-1-one | HCID 53488064 | — |
| Reactant | HCID 178418689 | HCID 178418689 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(5-Bromopyrimidin-2-yl)propan-2-ol | HCID 58485286 | 46.77% |
Reaction Steps
To a solution of 1-(5-bromopyrimidin-2-yl)ethanone (99 mg, 0.50 mmol) in THF (10 mL) was added MeMgBr (1.65 mL, 4.95 mmol) at −78° C. under nitrogen. The formed solution was stirred at −78° C. for 20 min, quenched with satd aq NH4Cl, and extracted with EtOAc. The combined organic layer was dried over anhydrous Na2SO4 and concentrated to give an oil, which was purified by prep TLC (3:1 PE/EtOAc) to give 2-(5-bromopyrimidin-2-yl)propan-2-ol (50 mg, yield: 46.77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569292B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-6601085bd313461aa1c2e3612db19e05 |
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| Source note | uspto-grants-2013_10 |
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