HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384391Generated: October 25, 2026
Bromine → 4-(3-Bromo-4-methoxyphenyl)pyridine
https://huagongshe.com/reaction/1384391
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | 4-(4-Methoxyphenyl)pyridine | HCID 603813 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-(3-Bromo-4-methoxyphenyl)pyridine | HCID 18476096 | — |
Reaction Steps
Bromine (26.0 g, 163 mmol) is added to a stirred solution of 4-(4-methoxyphenyl)pyridine (13.6 g. 73.5 mmol) in acetic acid (500 mL) and heated at 60° C. for 72 h. The mixture is then evaporated to dryness under reduced pressure and the residue is treated with aqueous ammonia (400 mL of 6M) and extracted with ethyl acetate (3×200 mL). The combined extracts are dried (Na2SO4), filtered and the solvent is evaporated off under reduced pressure to yield the crude product which is purified by chromatography (silica gel, 95% t-butylmethyl ether/4.5% methanol/0.5% aqueous NH3(25%)) and recrystallised from ether-cyclohexane to give 4-(3-bromo-4-methoxyphenyl)pyridine as a pale-yellow crystalline solid, m.p. 82-84° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06258843B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-95e315002c0145a79be5406ed4f4b68b |
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| Source note | uspto-grants-2001_07 |
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