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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624841Generated: October 25, 2026

Phosphorus oxychloride → Methyl 5-bromo-6-chloropicolinate

https://huagongshe.com/reaction/624841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantMethyl 5-bromopyridine-2-carboxylateHCID 7016458—
Reactant5-Bromo-2-(methoxycarbonyl)pyridine 1-oxideHCID 68458381—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-bromo-6-chloropicolinateHCID 4631119759%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 5-bromo-pyridine-2-carboxylic acid methyl ester (CAN 29682-15-3, 50 g, 0.23 mol) and m-CPBA (CAN 937-14-4, 80 g, 0.46 mol) in 400 mL dry methylene chloride was heated to 60° C. for 20 h. After that, the mixture was quenched with saturated sodium sulfite solution and extracted with ethyl acetate (2×200 mL). The organic layer was washed with brine (2×200 mL) and evaporated to dryness. The residue was purified with by column chromatography (silica gel, 300 g, eluting with 15% ethyl acetate in petroleum ether) to obtain a brown oil. The brown oil, 5-bromo-2-(methoxycarbonyl)pyridine 1-oxide (30 g, 0.13 mol) was added into phosphoryl trichloride (CAN 10025-87-3, 80 mL) at 0° C. over 1 h, then the mixture was heated to 95° C. for 1 h. After that the mixture was evaporated to dryness, the residue was dissolved in water (50 mL), extracted with ethyl acetate (3×50 mL) and the organic layer was evaporated to dryness to obtain the product as a white solid (19 g, 59%); MS (EI): m/e=249.9 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303012B2
Source datasetuspto-grants-2016_04
ORD IDord-d46354c48ad24083bb1f56a022aae737
Source noteuspto-grants-2016_04