Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072301Generated: November 1, 2026

Trisodium Phosphate → 3-Acetyl-5-bromopyridine

https://huagongshe.com/reaction/1072301

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 numberUS06909002B2
Source datasetuspto-grants-2005_06
ORD IDord-e8b92230f59a4fcfb7d68b2a9e5f5254
Source noteuspto-grants-2005_06