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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757834Generated: November 4, 2026

Acetyl chloride → 3-(Acetylamino)-5-(octadecyloxy)nitrobenzene

https://huagongshe.com/reaction/1757834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant3-Nitro-5-(octadecyloxy)benzenamineHCID 19388917—
SolventTetrahydrofuranHCID 8028—
Product3-(Acetylamino)-5-(octadecyloxy)nitrobenzeneHCID 1938902484%

Reaction Steps

To a solution d 1.4 g (3.44 mmol) of 3-nitro-5-(octadecyloxy)benzenamine and 0.75 ml (5.4 mmol) of triethylamine in 85 ml of THF stirred in an ice bath was added 0.25 ml (3.44 mmol) of acetyl chloride. The ice bath was removed after 15 minutes and the reaction mixture was stirred at room temperature for 17 hours. Triethylamine (0.3 ml) and acetyl chloride (0.15ml ) were added and stirring was continued for 5 hours. The solvent was removed at reduced pressure and the residue was crystallized from ethyl acetate-hexane to give 1.3 g (84% yield, mp 103°-107°) of 3-(acetylamino)-5-(octadecyloxy)nitrobenzene. The structure was confirmed by nmr and mass spectra.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446189
Source datasetuspto-grants-1995_08
ORD IDord-2c27bcf633944561b4c0ffa182eb7724
Source noteuspto-grants-1995_08