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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401635Generated: October 31, 2026

Bromine → 3-(Benzyloxy)-5-bromopyridin-2-amine

https://huagongshe.com/reaction/2401635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant2-Amino-3-benzyloxypyridineHCID 90334—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
Product3-(Benzyloxy)-5-bromopyridin-2-amineHCID 20626554—

Reaction Conditions

Temperature0 °C

Reaction Steps

200 g (1 mol) of 2-amino-3-benzyloxypyridine were initially charged in 4 l of dichloromethane, and a solution of 62 ml (1.2 mol) of bromine in 620 ml of dichloromethane was added at 0° C. over a period of 30 min. After the addition had ended, the reaction solution was stirred at 0° C. for 60 min. About 4 l of saturated aqueous sodium bicarbonate solution were then added to the mixture. The organic phase was separated off and concentrated. The residue was purified by silica gel column chromatography (petroleum ether:ethyl acetate 6:4) and the product fractions were concentrated. This gave 214 g (77% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796305B2
Source datasetuspto-grants-2014_08
ORD IDord-36a5eaaae9e14d4d99f8c27a7987bcb8
Source noteuspto-grants-2014_08