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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1819487Generated: October 30, 2026

2,5-Dichloropyridine-4-carbonitrile → N-(2,5-Dichloro-pyridin-4-ylmethyl)-acetamide

https://huagongshe.com/reaction/1819487

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Dichloropyridine-4-carbonitrileHCID 13560210—
ReactantAcOH AcOAcHCID 21895370—
CatalystAdams' catalystHCID 345198—
ProductN-(2,5-Dichloro-pyridin-4-ylmethyl)-acetamideHCID 5788554840%

Reaction Steps

A mixture of 3,6-dichloro-4-cyanopyridine (prepared according to WO 9633975) (3.40 g, 19.65 mmol) and PtO2 (0.40 g) in 1:1 Ac2O/AcOH (60 mL) was shaken in a Parr hydrogenation apparatus at 30 psi H2 for 6 h. The reaction mixture was filtered through a pad a celite and the filtered solids washed with EtOAc. The combined filtrate and washings were concentrated in vacuo and the resulting white solid purified by column chromatography on a 120 g ISCO combi-flash cartridge (silica gel, 20:80 to 100:0 EtOAc/hexane) to afford N-(2,5-Dichloro-pyridin-4-ylmethyl)-acetamide (1.73 g, 40%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601714B2
Source datasetuspto-grants-2009_10
ORD IDord-b346a9dbe47d444aa619666c90f2f766
Source noteuspto-grants-2009_10