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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387425Generated: October 26, 2026

Methanol → 4-Chloro-N-methylpicolinamide

https://huagongshe.com/reaction/387425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethylamineHCID 6329—
ReactantMethyl 4-chloropyridine-2-carboxylate--hydrogen chloride (1/1)HCID 16655470—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-N-methylpicolinamideHCID 147681480.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 17.8 g (0.103 mol, 1 eq) of 4-chloro-pyridine-2-carboxylic acid methyl ester hydrochloride in 15 mL, of methanol was cooled to 0° C. and slowly treated with a 2.0 M solution of methylamine in tetrahydrofuran at a rate that kept internal temperature below 5° C. The reaction mixture was stirred at 0° C. for 2 hours, then slowly allowed to warm up to ambient temperature and stirred for 18 hours. Solvent was removed in vacuum, approx. 200 mL of ethyl acetate was added and the resulting suspension was filtered. The precipitate was washed with 100 mL of ethyl acetate. The combined ethyl acetate solutions were washed three times with 100 mL of brine and dried over sodium sulfate. Solvent was removed in vacuum to yield 14.16 g of the product as orange oil. Yield: 80.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372971B2
Source datasetuspto-grants-2013_02
ORD IDord-a4e4c8b5a6254c1f8b5c73c2e6f29149
Source noteuspto-grants-2013_02