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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196074Generated: October 31, 2026

Acetic Anhydride → HCID 54243159, compound

https://huagongshe.com/reaction/1196074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
Reactant1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 54243159HCID 54243159—

Reaction Steps

N-Acetyl-N,N',N'-trimethylethylenediamine intermediate was prepared in the following manner. N,N,N'-Trimethylethylenediamine (24.5 g, 0.24 mol) was added to acetic anhydride (38 mL, 0.40 mol) over 1.5 hours with cooling in an ice-water bath. After stirring another 22 hours at ambient temperature, the reaction mixture was diluted with 50 mL of ether and 25 mL of water, and then cooled in an ice-water bath. A solution of 25 percent aqueous NaOH was added until the pH was approximately 10 and the phases were separated. The aqueous phase was extracted two more times with ether and the combined organic phase was concentrated on the rotary evaporator (50°,>100 mm Hg). Yield=2.4 g. The aqueous phase was saturated with NaCl and extracted again with methylene chloride (3×25 mL). After evaporation, it gave a total of 33.4 g of yellow liquid. Distillation through a 1×8 cm Vigreux column afforded 23.53 g of colorless liquid, bp 90°-1°/7 mm Hg (68 percent yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112920
Source datasetuspto-grants-1992_05
ORD IDord-59d9f7257b1a46a78863d9c9030a83c4
Source noteuspto-grants-1992_05