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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096997Generated: October 31, 2026

Acetic Anhydride → Hydrochloric Acid

https://huagongshe.com/reaction/1096997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantIsoamyl NitriteHCID 8053—
Reactant18-Crown-6HCID 28557—
ReactantSodium AcetateHCID 517045—
ReactantHydrochloride methanolHCID 21893726—
Reactant5-Ethoxy-2-methylanilineHCID 23369755—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductHydrochloric AcidHCID 313—
ProductHCID 66781995HCID 66781995—

Reaction Steps

In a 200-mL egg plant-type flask, acetic anhydride (9.46 mL, 100 mmol) was added to a CHCl3 solution (200 mL) of sodium acetate (5.89 g, 60 mmol) and 5-(ethyloxy)-2-methylaniline (8.96 g, 50 mmol), and stirred for 30 minutes with heating under reflux. Next, isoamyl nitrite (13.31 mL, 100 mmol) and 18-crown-6-ether (1.32 g, 5 mmol) were added to the reaction solution, and stirred overnight with heating under reflux. This was diluted with water, extracted with CHCl3, washed with aqueous saturated sodium hydrogencarbonate solution, and dried with sodium sulfate. The solution was filtered and concentrated to obtain a crude product. This was stirred in a hydrochloric acid/methanol solution at 60° C. for 30 minutes, and concentrated. The formed solid was washed with hexane and ethyl acetate to obtain the title compound of hydrochloride as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138197B2
Source datasetuspto-grants-2012_03
ORD IDord-c41da69d2f9c47b28dfd18b3051ab3dc
Source noteuspto-grants-2012_03