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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767185Generated: November 1, 2026

Ammonia → Methyl 6-bromopyridine-2-carboxylate

https://huagongshe.com/reaction/1767185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant6-Bromopyridine-2-carboxylic acidHCID 593919—
ProductMethyl 6-bromopyridine-2-carboxylateHCID 16217886—

Reaction Conditions

Temperature0 °C

Reaction Steps

6-Bromopyridine-2-carboxylic acid (6.000 g) was heated in refluxing methanol (180 mL) containing conc. sulphuric acid (2 mL) for 4 hrs. The reaction mixture was then cooled to ˜0° C. and conc. ammonia (4.8 mL) was added. The resulting solution was evaporated to give a white residue. This white solid was partitioned between brine and dichloromethane (100/100 mL). After thorough shaking the organic layer was dried (magnesium sulphate) and evaporated to give a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07232821B2
Source datasetuspto-grants-2007_06
ORD IDord-1d2be00d738e44ccba8a9553e59a0153
Source noteuspto-grants-2007_06