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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456281Generated: October 30, 2026

Acetic Anhydride → HCID 66811912, compound

https://huagongshe.com/reaction/456281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactantp-(Trifluoromethoxy)benzaldehydeHCID 69573—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
ReactantHCID 66812088HCID 66812088—
SolventEthanolHCID 702—
SolventHexaneHCID 8058—
ProductHCID 66811912HCID 6681191270%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of N-(4-{2-[4-(dimethylamino)phenyl]ethoxy}benzoyl)glycine (241 mg, 0.676 mmol) prepared in Example 23 (23b), 4-(trifluoromethoxy)benzaldehyde (106 pt, 0.742 mmol), sodium acetate (83.9 mg, 1.02 mmol), and acetic anhydride (319 μL, 3.38 mmol) was stirred at 120° C. for 15 minutes and then allowed to cool to room temperature. A saturated sodium hydrogen carbonate aqueous solution, hexane, and ethanol were added to the resulting solidified product which was washed by ultrasonic vibration. The precipitate was collected by filtration and dried by heating under reduced pressure to give 234 mg of the title compound (orange solid, yield: 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497397B2
Source datasetuspto-grants-2013_07
ORD IDord-479fca27f3eb417fb02377d4bc630a97
Source noteuspto-grants-2013_07