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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066884Generated: November 3, 2026

Acetic Anhydride → N-Benzyl-N-((E)-but-1-enyl)-acetamide

https://huagongshe.com/reaction/2066884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantBenzyl-((E)-but-1-enyl)-amineHCID 15360338—
SolventTolueneHCID 1140—
ProductN-Benzyl-N-((E)-but-1-enyl)-acetamideHCID 13494620—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 62a (3.22 g, 20 mmol) in 10 mL of toluene, was added triethylamine (2.79 mL, 20 mmol). The mixture was cooled to 0° C. and acetic anhydride (1.89 mL, 20 mmol) was added dropwise. The mixture was warmed to room temperature and stirred overnight. It was then concentrated on high vacuum to give crude 62b.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293729B2
Source datasetuspto-grants-2012_10
ORD IDord-cd85b76f62644e16b5d6b84171cc7b09
Source noteuspto-grants-2012_10