HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620889Generated: October 25, 2026
Hydrochloric Acid → 3-hydroxy-N-[5-(methylsulfinyl)-1,3-thiazol-2-yl]benzamide
https://huagongshe.com/reaction/1620889
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-{[5-(Methylsulfinyl)-1,3-thiazol-2-yl]carbamoyl}phenyl acetate | HCID 56969394 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-hydroxy-N-[5-(methylsulfinyl)-1,3-thiazol-2-yl]benzamide | HCID 56969396 | — |
Reaction Steps
2 M hydrochloric acid (40.0 mL) is added to a suspension of 8 (0.370 g, 1.13 mmol) in tetrahydrofuran (17.0 mL), and the reaction is warmed to reflux. The reaction becomes homogeneous upon heating. After refluxing for 4 hours, the reaction is allowed to cool to room temperature, and is concentrated in vacuo. The residue is suspended in water and filtered. The filter pad is washed with water, air dried, and then re-dissolved in a minimum amount of warm THF. Water is added to the warm THF solution until the solution turns turbid, and the resulting mixture is allowed to cool to room temperature. Additional water is added, and a white solid forms on standing. The crystalline product is filtered, and the filter pad is washed with water, and dried in vacuo at 70° C. and gives 10 as a white crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772502B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-1efcfe6a2d384f478d1e037c16ebe4b6 |
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| Source note | uspto-grants-2014_07 |
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