HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330803Generated: October 25, 2026
tert-Butyl methyl ether → (3-(5-Bromopyrimidin-2-yl)phenyl)methanol
https://huagongshe.com/reaction/330803
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | [3-(Hydroxymethyl)phenyl]boronic acid | HCID 2734662 | — |
| Reactant | 5-Bromo-2-iodopyrimidine | HCID 7006651 | — |
| Reactant | Tripotassium phosphate trihydrate | HCID 18407952 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (3-(5-Bromopyrimidin-2-yl)phenyl)methanol | HCID 59484879 | — |
Reaction Steps
750 mg (0.65 mmol) of tetrakis(triphenylphosphine)palladium are added to a solution, kept under nitrogen, of 6.11 g (21.5 mmol) of 5-bromo-2-iodo-pyrimidine, 3.91 g (25.7 mmol) of 3-(hydroxymethyl)benzeneboronic acid and 9.11 g (42.9 mmol) of tripotassium phosphate trihydrate in 120 ml of dioxane and 14 ml of water, and the mixture is stirred at 90° C. for 18 hours. The reaction mixture is cooled to room temperature, tert-butyl methyl ether and water are added, and the mixture is filtered through kieselguhr. The organic phase of the filtrate is separated off, dried over sodium sulfate and evaporated. The residue is chromatographed on a silica-gel column with dichloromethane/methanol as eluent; product: 2.49 g;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877751B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-5f83a13a72554b6d8bc07ea54d0e89dc |
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| Source note | uspto-grants-2014_11 |
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