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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333861Generated: October 26, 2026

Water → 2-(2,4-Dichloro-phenyl)-3-(6-methoxy-pyridin-3-yl)-3-oxo-propionitrile

https://huagongshe.com/reaction/333861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,4-DichlorophenylacetonitrileHCID 80566—
ReactantMethyl 6-methoxypyridine-3-carboxylateHCID 586039—
Solventtert-ButanolHCID 6386—
Product2-(2,4-Dichloro-phenyl)-3-(6-methoxy-pyridin-3-yl)-3-oxo-propionitrileHCID 6681311629.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a suspension of potassium-tert-butylate (2.052 g) in tert-butanol (25 ml) was added methyl-6-methoxynicotinate (2.5 g). 2,4-Dichlorobenzyl cyanide (2.782 g) was added portion wise. The mixture was heated to 100° C. for 1.5 h. After cooling to room temperature, water (100 ml) was added and the mixture was washed with diethyl ether. The aqueous phase was neutralized with concentrated aqueous HCl and extracted with EtOAc. The organic phase was washed with water and with brine, dried (MgSO4), filtered and concentrated to dryness to give the title compound (1.407 g) as a yellow foam that was used in the next step without further purification. MS (m/e)=321.0 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883786B2
Source datasetuspto-grants-2014_11
ORD IDord-9dcae863c2d24463ae9abf9130636ceb
Source noteuspto-grants-2014_11