Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371179Generated: October 30, 2026

Dimethylcarbamoyl Chloride → Bis(5-chloropyridin-2-yl)methanone

https://huagongshe.com/reaction/371179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylcarbamoyl ChlorideHCID 6598—
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Bromo-5-chloropyridineHCID 817098—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductBis(5-chloropyridin-2-yl)methanoneHCID 2027451927%

Reaction Conditions

Temperature-70 °C

Reaction Steps

A solution of n-butyllithium in hexane (16.3 ml, 1.55 molar) was added under nitrogen to a stirred solution of 2-bromo-5-chloropyridine (5 g) in dry diethyl ether (70 ml) at -70° C. over a period of 20 minutes. A solution of dimethylcarbamoylchloride (1.36 g) in dry diethyl ether (25 ml) was then added slowly over a period of 20 minutes. The mixture was stirred for a further 20 minutes at -70° C. and a solution of ammonium chloride (5 g) in water (50 ml) was then added and the solution allowed to warm to room temperature. The ether layer was separated and the aqueous solution extracted with diethyl ether (2×50 ml). The ether extracts were combined, dried over magnesium sulfate and evaporated. The residue was chromatographed on silica, eluting with a mixture of ethyl acetate and petroleum ether b.p. 60°-80° C. (1:9). The relevant fractions were combined and evaporated and the residue triturated with diethyl ether and dried to yield the title compound as a buff colored solid (0.86 g), (27%), m.p. 164°-167° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04529799
Source datasetuspto-grants-1985_07
ORD IDord-d0f653908ba94d40b4f09f8ef782d0aa
Source noteuspto-grants-1985_07