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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389263Generated: October 29, 2026

Acetic Anhydride → N-Benzyl-N-(prop-1-en-1-yl)acetamide

https://huagongshe.com/reaction/389263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 178457043HCID 178457043—
ProductN-Benzyl-N-(prop-1-en-1-yl)acetamideHCID 9942349—

Reaction Conditions

Temperature0 °C

Reaction Steps

To benzyl-prop-(E)-ylidene-amine (6.0 g, 40 mmol) in triethylamine (5.67 mL, 40 mmol) at 0° C. was slowly added acetic anhydride (3.81 mL, 40 mmol), and the reaction was stirred for 30 minutes at 0° C. and then overnight at room temperature. The mixture was concentrated, and the residue was purified by silica gel chromatography (0-25% EtOAc in hexanes) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378107B2
Source datasetuspto-grants-2013_02
ORD IDord-62296e56bb704f65856518b390e5b164
Source noteuspto-grants-2013_02