Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907820Generated: October 31, 2026

Trifluoroacetic anhydride → HCID 58137374, compound

https://huagongshe.com/reaction/1907820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 58137375HCID 58137375—
SolventDichloromethaneHCID 6344—
ProductHCID 58137374HCID 58137374—

Reaction Steps

3,4-Diethoxy-6-methylpyridazine 1-oxide (1.44 g) was initially charged in dichloromethane (50 ml) and admixed dropwise at RT with trifluoroacetic anhydride (2.5 ml). After 2.5 h, the mixture was concentrated to dryness and the residue was taken up with ethanol and saturated potassium carbonate solution. After stirring at RT for 4 h, the mixture was concentrated to dryness again and the residue was admixed with water and dichloromethane. Removal of the organic phase was followed by extraction twice more with dichloromethane, and the combined organic phases were dried over magnesium sulfate, filtered and concentrated. The residue was purified twice using silica gel with dichloromethane/methanol as the eluent. The product-containing fractions were combined and dried. 716 mg of the desired product were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598177B2
Source datasetuspto-grants-2013_12
ORD IDord-3dcfb6ad95974df29e5c5834076b3228
Source noteuspto-grants-2013_12