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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714127Generated: November 4, 2026

Ammonium Chloride → 1-{6-[1-(2-Chloro-4,6-dimethylphenylimino)ethyl]pyridin-2-yl}ethanone

https://huagongshe.com/reaction/1714127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantDimethylacetamideHCID 31374—
ReactantHCID 57539554HCID 57539554—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product1-{6-[1-(2-Chloro-4,6-dimethylphenylimino)ethyl]pyridin-2-yl}ethanoneHCID 5946462447%

Reaction Conditions

Temperature-70 °C

Reaction Steps

2.00 g (0.0059 mol) of [1-(6-bromopyridin-2-yl)ethylidene](2-chloro-4,6-dimethylphenyl)amine were dissolved in 25 ml of diethyl ether and cooled to −70° C. 3.70 ml (0.0059 mol) of a 1.6 M solution of butyllithium in hexane were added dropwise over a period of 15 minutes. The temperature rose to −40° C. and the mixture was stirred for another 30 minutes. The mixture was cooled to −70° C. and 0.52 g (0.0059 mol) of N,N-dimethylacetamide was added dropwise and the mixture was stirred at room temperature for another three hours. The reaction mixture was stirred with 5 ml of a saturated ammonium chloride solution. The aqueous phase was extracted twice with diethyl ether. The combined organic phases were dried over Na2SO4, filtered and the solvent was distilled off under reduced pressure. This gave 0.83 g (0.0028 mol) of the product in a yield of 47%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795441B2
Source datasetuspto-grants-2010_09
ORD IDord-765db60613ea4a2bb39f120c68aee76d
Source noteuspto-grants-2010_09