HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295949Generated: October 29, 2026
Water → 4-[(5-Bromo-2-pyrimidinyl)oxy]phenol
https://huagongshe.com/reaction/2295949
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 5-bromo-2-(4-methoxyphenoxy)pyrimidine | HCID 4541513 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[(5-Bromo-2-pyrimidinyl)oxy]phenol | HCID 13336640 | 92.1% |
Reaction Steps
5-Bromo-2-(4-methoxyphenoxy)pyrimidine (2.4 g) was dissolved in methylene chloride (50 ml) and the solution cooled to a temperature of -70° C. Boron tribromide (12.7 g) was added dropwise to the stirred solution, the temperature of the solution being maintained at -65° to -75° C. On completion of the addition the reaction mixture was stirred for a further one hour at a temperature of -65° to -75° C. and then the temperature of the reaction mixture was allowed to rise slowly to room temperature. The reaction mixture was added cautiously, in small portions, to water and the methylene chloride removed by heating the mixture on a water bath. The aqueous suspension was cooled to a temperature of 20° C., the solid was collected by filtration, washed with water and recrystallised from methanol/water to give 4-(5-bromo-2-pyrimidyloxy)phenol (2.1 g) m.p. 178° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04427437 |
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| Source dataset | uspto-grants-1984_01 |
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| ORD ID | ord-262a7d94efc04ad4bb8c16f2400f7347 |
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| Source note | uspto-grants-1984_01 |
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