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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524762Generated: October 31, 2026

Acetic Anhydride → HCID 90043370, compound

https://huagongshe.com/reaction/524762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant4-(Trifluoromethyl)thiazole-2-carbonitrileHCID 59533434—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 90043370HCID 9004337087.1%

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340538B2
Source datasetuspto-grants-2016_05
ORD IDord-cb347c5867d74340b3809c9dc158934b
Source noteuspto-grants-2016_05