Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | N-[4-(Hydroxymethyl)-1,3-thiazol-2-YL]acetamide | HCID 14931748 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 15729141 | HCID 15729141 | 86.9% |
Reaction Steps
A mixture of 2-acetylamino-4-hydroxymethylthiazole (7.0 g) and N-chlorosuccinimide (6.5 g) in acetic acid (70 ml) was heated at 40° C. for 3.5 hours with stirring. The reaction mixture was concentrated under reduced pressure and the residue was added the aqueous sodium bicarbonate. The mixture was extracted with a mixture of ethyl acetate and tetrahydrofuran (1:1), washed with water and dried over magnesium sulfate. The solvent was concentrated under reduced pressure and the residue was triturated with isopropyl ether. The precipitates were collected by filtration, washed with isopropyl ether and dried in vacuo to give 2-acetylamino-5-chloro-4-hydroxymethylthiazole (7.3 g, yield : 78.5%). mp: 145°-146° C. IR (Nujol) : 3150, 1690, 1550, 1285 cm-1
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05256675 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-f2909747712545b5be30f6c15e0ef389 |
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| Source note | uspto-grants-1993_10 |
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