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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907060Generated: November 3, 2026

Acetic Anhydride → HCID 322651, compound

https://huagongshe.com/reaction/1907060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantPotassium HydroxideHCID 14797—
ReactantL-Glutamic AcidHCID 33032—
ProductHCID 322651HCID 322651—

Reaction Conditions

Temperature60 °C

Reaction Steps

A 500-mL round bottom flask under argon atmosphere is charged with L-glutamic acid 4 (21 g, 0.143 mol), a catalytic amount of N,N-dimethylaminopyridine (150 mg, 1×10−3 mol), acetic anhydride (75 mL) and triethylamine previously distilled over KOH (75 mL). The reaction mixture is maintained at 60° C. for 16 hours. The progression of the reaction is followed by TLC (eluent: ethyl acetate/petroleum ether at a ratio of 8/2). The crude reaction product is concentrated under reduced pressure (rotary evaporator and vane pump) and then taken up in 200 mL of dichloromethane; the organic layer is then washed five times with 100 mL of deionized water and then treated over animal carbon. The product obtained after evaporation of the solvent is purified by crystallization from petroleum ether/CH2Cl2. The crystals are rinsed with petroleum ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08597706B2
Source datasetuspto-grants-2013_12
ORD IDord-699c755f0bcd49e6a5a52772460cd458
Source noteuspto-grants-2013_12