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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31393Generated: October 28, 2026

Methanol → Methyl 3-bromoisonicotinate Hydrochloride

https://huagongshe.com/reaction/31393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant3-Bromoisonicotinic Acid HydrochlorideHCID 68430687—
CatalystDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductMethyl 3-bromoisonicotinate HydrochlorideHCID 68433567—

Reaction Steps

To a stirred suspension of 3-bromoisonicotinic acid hydrochloride (27.4 g, 0.10 mol) in ethyl acetate (250 ml) was added one drop of DMF followed by thionyl chloride (18.5 g, 0.16 mol). The mixture was heated at reflux for 1 h and allowed to cool to room temperature. The mixture was then concentrated under reduced pressure to give an off-white solid. To this was added methanol and this was refluxed for 2 hrs. The mixture was then concentrated under reduced pressure and diluted with ethyl acetate. The precipitate was collected on filter paper on a Buchner funnel. The white solid was washed with ethyl acetate and air-dried. The white solid was placed in a vacuum oven at 60° C. overnight with a nitrogen bleed. Yield: 18.5 g (71% th).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425639B2
Source datasetuspto-grants-2008_09
ORD IDord-12017e20021f467a8b28a740c514cdfb
Source noteuspto-grants-2008_09