HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524762Generated: October 31, 2026
Acetic Anhydride → HCID 90043370, compound
https://huagongshe.com/reaction/524762
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 4-(Trifluoromethyl)thiazole-2-carbonitrile | HCID 59533434 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 90043370 | HCID 90043370 | 87.1% |
Reaction Steps
To a solution of 4-(trifluoromethyl)thiazole-2-carbonitrile (0.9 g, 5 mmol) and TEA (1.1 mL, 7.5 mmol) in DCM (20 mL) was added hydroxylamine hydrochloride (0.35 g, 5 mmol), then the mixture was stirred at 25° C. for 2 hours. The mixture was concentrated in vacuo and the residue was purified by a silica gel column chromatography (PETROLEUM ETHER/EtOAc (V/V)=10/1) to give the crude product as a white solid. To the white solid in acetic acid (25 mL) were added Ac2O (0.32 mL, 3.33 mmol) and Pd—C (10%, 0.2 g), then the mixture was stirred at 25° C. for 12 hours under N2. The reaction mixture was filtered and the filtrate was concentrated in vacuo. Then the residue was crystallized from EtOAc (2 mL) and ether (10 mL) to give the title compound as a white solid (0.74 g, 58%). The compound was characterized by the following spectroscopic data:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09340538B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-cb347c5867d74340b3809c9dc158934b |
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| Source note | uspto-grants-2016_05 |
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