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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dichloroacetone | HCID 10793 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(Dimethylamino)ethanethioamide | HCID 3032838 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 1-(4-(chloromethyl)thiazol-2-yl)-N,N-dimethylmethanamine hydrochloride | HCID 13121958 | 136% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09163006B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-f8fe967cbd1d44608ea55e9b13fdb606 |
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| Source note | uspto-grants-2015_10 |
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