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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632143Generated: October 26, 2026

Water → Methyl 5-bromo-6-(cyclopropylmethoxy)picolinate

https://huagongshe.com/reaction/632143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium CarbonateHCID 10340—
Reactant5-Bromo-6-cyclopropylmethoxy-pyridine-2-carboxylic acidHCID 71087543—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-bromo-6-(cyclopropylmethoxy)picolinateHCID 7108728648%

Reaction Steps

A solution of 5-bromo-6-(cyclopropylmethoxy)-pyridine-2-carboxylic acid (Example 9 d, 0.4 g, 1.5 mmol), iodomethane (CAN 16519-98-5, 0.42 g, 3 mmol), sodium carbonate (0.16 g, 1.5 mmol) in DMF (10 mL) was stirred overnight at room temperature. Water was poured into the reaction solution and the resulting mixture was extracted with ethyl acetate (3×30 mL). The combined organic extracts were washed with water and brine, dried over anhydrous sodium sulfate and evaporated. The residue was purified by column chromatography (silica gel, 20 g, 5% ethyl acetate in petroleum ether) to yield the title compound (0.2 g, 0.7 mmol, 48%) as white solid; MS (EI): m/e=286.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321727B2
Source datasetuspto-grants-2016_04
ORD IDord-983252f5a99e4e5fa5c9ea38e8da3c46
Source noteuspto-grants-2016_04