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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525537Generated: October 30, 2026

Potassium Carbonate → N-(5-Bromo-pyridin-2-ylmethyl)-O-methyl-hydroxylamine

https://huagongshe.com/reaction/525537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
Reactant5-bromo-2-(chloromethyl)pyridineHCID 11401501—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-(5-Bromo-pyridin-2-ylmethyl)-O-methyl-hydroxylamineHCID 7895562728.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of 5-Bromo-2-chloromethyl-pyridine (2 g, 9.709 mmol) in dimethylformamide (30 mL) is added methoxy amine hydrochloride salt (0.973 g, 11.65 mmol) and K2CO3 (3.35 g, 24.27 mmol) at room temperature then heated to 60° C. for 16 hours. Reaction mixture diluted with water and extracted with ethyl acetate. Organic layer is dried over sodium sulphate, solvent is evaporated in vacuo and purified by combiflash using 30% ethyl acetate in hexane as an eluent to afford the title compound (0.6 g). 1HNMR (400 MHz, DMSO-d6) δ: 3.36 (s, 3H), 3.99 (d, J=5.88 HZ, 2H), 7.10 (t, 1H), 7.44-7.46 (dd, J1=8.32 Hz, J2=0.32 Hz, 1H), 7.99-8.02 (dd, J1=2.44 Hz, J2=8.4 Hz, 1H), 8.60-8.61 (dd, J1=2.4 Hz, J2=0.4 Hz, 1H). LC-MS (m/z): [M+H]=217.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340564B2
Source datasetuspto-grants-2016_05
ORD IDord-e41d4a67e0b0487a91f13723c38be11a
Source noteuspto-grants-2016_05