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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848250Generated: November 2, 2026

Allyl bromide → HCID 86681223, compound

https://huagongshe.com/reaction/1848250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178507942HCID 178507942—
SolventDimethylformamideHCID 6228—
ProductHCID 86681223HCID 8668122316.3%

Reaction Steps

To a stirred solution of 2-aminopyridin-4-ol (500 mg, 4.5 mmol) in DMF (5 mL) at rt was added K2CO3 (940 mg, 6.8 mmol). The resulting mixture was stirred at rt for 20 min before allyl bromide (393 μL, 4.5 mmol) was added. The mixture was then stirred at rt overnight and heated at 60° C. for 2 h. After cooling to rt, the mixture was partitioned between EtOAc and water, and the organic layer was washed with brine, dried over Na2SO4, and evaporated under reduced pressure. The residue was purified by silica gel chromatography eluting with EtOAc in hexanes to give 4-(allyloxy)pyridin-2-amine (110 mg, 16%) as a white solid. LCMS (ESI) m/z 151 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952058B2
Source datasetuspto-grants-2015_02
ORD IDord-8c5cf9e58bcb4beba3a9fba38813cc03
Source noteuspto-grants-2015_02