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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230803Generated: October 30, 2026

Trifluoroacetic anhydride → HCID 69004389, compound

https://huagongshe.com/reaction/230803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 69002568HCID 69002568—
SolventDichloromethaneHCID 6344—
ProductHCID 69004389HCID 6900438983.7%

Reaction Conditions

Temperature40 °C

Reaction Steps

Trifluoroacetic anhydride (3 mL) was added to a dichloromethane solution (6 mL) of ethyl 5-[2-{[(4-methylphenyl)sulfonyl]imino}-5-nitropyridin-1(2H)-yl]-4-oxohexanoate (635 mg) obtained in Production Example 47-4, at room temperature. The reaction liquid was heated up to 40° C., stirred for 6 hours, and then concentrated under reduced pressure. Aqueous saturated sodium hydrogencarbonate solution was added to the residue, and extracted with ethyl acetate. The organic layer was dried with sodium sulfate, concentrated under reduced pressure, and the residue was purified through silica gel column chromatography (ethyl acetate/chloroform/hexane=1/1/1) to obtain the entitled compound (328 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566781B2
Source datasetuspto-grants-2009_07
ORD IDord-6e78c1c7087a40a68b3a5e5757c30779
Source noteuspto-grants-2009_07