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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911035Generated: October 30, 2026

Bromine → Ethyl 3-(2-amino-5-bromopyridin-4-yloxy)-4-chlorobenzoate

https://huagongshe.com/reaction/911035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantEthyl 3-(2-aminopyridin-4-yloxy)-4-chlorobenzoateHCID 66617829—
SolventAcetic AcidHCID 176—
ProductEthyl 3-(2-amino-5-bromopyridin-4-yloxy)-4-chlorobenzoateHCID 6661781061.4%

Reaction Steps

A flask was charged with ethyl 3-(2-aminopyridin-4-yloxy)-4-chlorobenzoate (5.50 g, 18.8 mmol) and acetic acid (50 mL), and bromine (0.943 ml, 18.4 mmol) was added. The reaction was stirred at ambient temperature for 30 minutes and then concentrated. The residue was purified by silica gel column chromatography, eluting with 20%-35% ethyl acetate in hexanes to give the desired product (4.20 g, 58.9% yield) as light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022222B2
Source datasetuspto-grants-2011_09
ORD IDord-acb1015a38cd4fb2a8527bc7d186e04d
Source noteuspto-grants-2011_09