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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752364Generated: October 28, 2026

1,3-Dichloroacetone → 1-(4-(chloromethyl)thiazol-2-yl)-N,N-dimethylmethanamine hydrochloride

https://huagongshe.com/reaction/1752364

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DichloroacetoneHCID 10793—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(Dimethylamino)ethanethioamideHCID 3032838—
Solvent1,2-DichloroethaneHCID 11—
Product1-(4-(chloromethyl)thiazol-2-yl)-N,N-dimethylmethanamine hydrochlorideHCID 13121958136%

Reaction Conditions

Temperature70 °C

Reaction Steps

2-(Dimethylamino)ethanethioamide (0.382 g, 3.24 mmol), 1,3-dichloroacetone (0.453 g, 3.56 mmol) and sodium bicarbonate (0.301 g, 3.56 mmol) was stirred in 1,2-dichloroethane (4 mL) at room temperature for 24 h. The reaction mixture was filtered and the filter cake was washed with 1,2-dichloroethane. The filtrate was added dropwise to a cooled (ice bath) solution of thionyl chloride (0.260 mL, 3.56 mmol) in 1,2-dichloroethane (2 mL). The solution was stirred at 70° C. for 0.5 h and then cooled to room temperature. The brown mixture was filtered and washed with 1,2-dichloroethane to afford N-{[4-(chloromethyl)-1,3-thiazol-2-yl]methyl}-N,N-dimethylamine hydrochloride as a brown solid (0.550 g, 2.42 mmol, 75% yield). 1H NMR (400 MHz; D2O): 2.79 (s, 6H); 4.52 (s, 2H); 4.61 (s, 2H); 7.60 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09163006B2
Source datasetuspto-grants-2015_10
ORD IDord-f8fe967cbd1d44608ea55e9b13fdb606
Source noteuspto-grants-2015_10