Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131153Generated: October 25, 2026

Hydrochloric Acid → 2-Chloro-1-(4-methyl-3-pyridinyl)ethanone hydrochloride

https://huagongshe.com/reaction/131153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChlorosuccinimideHCID 31398—
Reactant1-(4-Methyl-3-pyridinyl)ethanoneHCID 10942481—
ReactantEther hydrochlorideHCID 10953452—
SolventDiethyl EtherHCID 3283—
SolventAcetate-hydrochloric acidHCID 22641269—
Product2-Chloro-1-(4-methyl-3-pyridinyl)ethanone hydrochlorideHCID 2186494483.2%

Reaction Steps

In a 500 mL round bottom flask was placed 1-(4-methyl-3-pyridinyl)ethanone (10.0 g, 74.1 mmol) in 90 mL of Et2O. To this solution was added 88.9 mL of 1M HCl/Et2O (1.2 eq, 88.9 mmol) with stirring and the solution allowed to stir for 1 h at room temperature, at which point, the precipitate was filtered and washed with Et2O. The solid was then dried in vacuo at about 60° C. This HCl salt (12. g, 70.0 mmol) was then dissolved in 70.0 mL of 1M HCl/acetic acid where 9.34 g (1 eq, 70.0 mmol) of N-chlorosuccinimide (NCS) was added and the reaction allowed to stir under Argon at room temperature overnight. At this point, 300 mL of Et2O was added resulting in an off-white precipitate. This was allowed to stir for 1 h at which point the solid was filtered and rinsed with Et2O to provide 12.0 g (83%) of the desired 2-chloro-1-(4-methyl-3-pyridinyl)ethanone hydrochloride. 1H-NMR (DMSO-d6) δ 2.51 (s, 3H), 5.15 (s, 2H), 7.68 (d, 1H), 8.68 (d, 1H), 9.06 (s, 1H); MS GC-MS [MH]+ 169.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384947B2
Source datasetuspto-grants-2008_06
ORD IDord-f3f0c771de66486cbf44449a29c86d47
Source noteuspto-grants-2008_06