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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624074Generated: October 25, 2026

Sulfuric Acid → 5-Bromo-3-[(2,6-difluorobenzyl)oxy]pyridine-2-amine

https://huagongshe.com/reaction/1624074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantBromineHCID 24408—
Reactant3-(2,6-Difluoro-benzyloxy)-pyridin-2-ylamineHCID 10263498—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product5-Bromo-3-[(2,6-difluorobenzyl)oxy]pyridine-2-amineHCID 21111488—

Reaction Conditions

Temperature0 °C

Reaction Steps

32.6 g of 3-[(2,6-difluorobenzyl)oxy]pyridine-2-amine (Example 4A; 138 mmol, 1 equivalent) were suspended in 552 ml of 10% strength sulphuric acid, and the mixture was cooled to 0° C. 8.5 ml of bromine (165 mmol, 1.2 equivalents) were dissolved in 85 ml of acetic acid and then, over a period of 90 min, added dropwise to the ice-cooled reaction solution. After the dropwise addition had ended, the mixture was stirred at 0° C. for 90 min and then diluted with 600 ml of ethyl acetate, and the aqueous phase was separated off. The aqueous phase was re-extracted with ethyl acetate and the organic phases were combined, washed with saturated aqueous sodium bicarbonate solution, dried and concentrated. The residue was dissolved in dichloromethane and chromatographed on silica gel (petroleum ether/ethyl acetate gradient as mobile phase). This gave 24 g (55% of theory) of the title compound. LC-MS (Method 1): Rt=0.96 min

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778964B2
Source datasetuspto-grants-2014_07
ORD IDord-fc0f3bd793774287ae423a62a0b068f9
Source noteuspto-grants-2014_07