HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940883Generated: October 30, 2026
1,3-Dichloroacetone → 2-Acetoxymethyl-4-chloromethyl-4-hydroxythiazoline hydrochloride
https://huagongshe.com/reaction/1940883
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dichloroacetone | HCID 10793 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Carbamothioylmethyl acetate | HCID 11018908 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 2-Acetoxymethyl-4-chloromethyl-4-hydroxythiazoline hydrochloride | HCID 21464456 | 60% |
Reaction Steps
A mixture of 5.33 g of 2-acetoxythioacetamide, prepared according to Example 2, 5.21 g of 1,3-dichloroacetone, 3.44 g of sodium bicarbonate and 20 ml of 1,2-dichloroethane was heated at 40° C. for 15 hours. The mixture was filtered to remove insoluble inorganics and concentrated under reduced pressure to an oil. The oil was taken up in 25 ml of isopropyl alcohol saturated with hydrogen chloride (5N) and 25 ml of isopropanol added to improve stirring. The slurry was stirred for 30 minutes at 0° C. and then filtered. The precipitate was washed with cold IPA and dried at room temperature under reduced pressure. The product 2-acetoxymethyl-4-chloromethyl-4-hydroxythiazoline hydrochloride was obtained in 60% yield (1.66 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05700945 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-946de4f18da74aaf9ca9ffb2198ed721 |
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| Source note | uspto-grants-1997_12 |
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