HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212869Generated: October 26, 2026
Bromine → 2-Bromo-2-[2-(methylthio-4-pyrimidinyl)]-1-phenylethanone
https://huagongshe.com/reaction/2212869
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2-[2-(Methylsulfanyl)pyrimidin-4-yl]-1-phenylethan-1-one | HCID 12985829 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Bromo-2-[2-(methylthio-4-pyrimidinyl)]-1-phenylethanone | HCID 12985830 | — |
Reaction Steps
Bromine (24.1 g, 0.15 mol) is added with stirring to 2-(2-methylthio-pyrimidin-4-yl)-1-phenyl-ethanone (36.8 g, 0.15 mol) in acetic acid (300 ml) in such a way that the reaction temperature does not exceed +25° C. and the color of the bromine is discharged immediately. After the addition of the bromine solution the solvent is removed by evaporation under vacuum. The pH of the resulting oil is adjusted to 8 using an aqueous saturated sodium bicarbonate solution and the product is extracted several times with diethylther. Drying the combined extracts with magnesium sulfate, filtering and evaporation of the solvent gives the crude 2-bromo-2-(2-methylthio-pyrimidin-4-yl)-1-phenyl-ethanone in form of an oil of sufficient purity for the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07105517B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-7247a1ba44ba47bda4393e8b1fbc9a89 |
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| Source note | uspto-grants-2006_09 |
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