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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989244Generated: November 1, 2026

Acetic Anhydride → HCID 67393385, compound

https://huagongshe.com/reaction/1989244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178449977HCID 178449977—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHCID 67393385HCID 67393385148%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a mixture of 6-(3-tert-butylsulfamoyl-phenyl)-N-hydroxy-pyridine-2-carboxamidine (Example C.7) (830 mg, 2.38 mmol) in acetic acid (10 ml) at 23° C. was added acetic anhydride (0.34 ml, 3.57 mmol) and the mixture was stirred at 23° C. for 10 min, then 10% Pd on charcoal (84 mg, 0.79 mmol) was added and the mixture was hydrogenated (1 bar hydrogen) at 23° C. for 24 h. The catalyst was filtered off, washed with acetic acid and the solvents were evaporated to give the title compound (1.38 g, 148%, contains excess acetic acid) as a light yellow oil, which was used without further purification (cf. Synth. Commun. 1996, 26(23), 4351). MS (ISP) 333.1 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642264B2
Source datasetuspto-grants-2010_01
ORD IDord-7f7865cc30d34989a002cefdcc3598da
Source noteuspto-grants-2010_01