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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839148Generated: November 1, 2026

Trisodium Phosphate → 3-Acetyl-5-bromopyridine

https://huagongshe.com/reaction/1839148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrisodium PhosphateHCID 24243—
ReactantEthyl 5-bromopyridine-3-carboxylateHCID 140785—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
Product3-Acetyl-5-bromopyridineHCID 820423—

Reaction Steps

To a solution of ethyl 5-bromonicotinate (3.9 g, 16.9 mmol) in ether (50 ml) at 0° C. was added a 3M solution of methylmagnesium bromide (16.9 ml, 50.8 mmol). The resulting thick slurry was warmed slowly to room temperature and after 1.5 hours it was poured slowly into an excess of 1M aqueous monobasic sodium phosphate. The mixture was partitioned between ether and water and the product from the organic phase was chromatographed on silica gel, eluting with a 1:1:2 mixture of ether, pentane and ammonia-saturated methylene chloride to afford the 3-acetyl-5-bromopyridine compound. This preparation also afforded 3-bromo-5-(1-hydroxy-1-methylethyl)pyridine described in Example 25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677351B2
Source datasetuspto-grants-2004_01
ORD IDord-044289f79fcc49d892cfc08a5dcc1c9b
Source noteuspto-grants-2004_01