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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395225Generated: October 25, 2026

Chloroacetyl chloride → Acetamide, N-(5-hydroxy-1-naphthalenyl)-

https://huagongshe.com/reaction/395225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantCalcium CarbonateHCID 10112—
Reactant5-Amino-1-naphtholHCID 65746—
Solvent1,4-DioxaneHCID 31275—
ProductAcetamide, N-(5-hydroxy-1-naphthalenyl)-HCID 8965376%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 5-amino-1-naphthol (17.6 g; 0.11 mol) in 500 ml of dioxane, there were added 11 g of calcium carbonate (0.11 mol) and, dropwise, 8 ml of chloroacetyl chloride (0.112 mol), with stirring and under an inert atmosphere. The reaction medium was heated at 80° C. for 2 hours 30 minutes. The suspension was cooled to room temperature, filtered on sintered glass and the inorganic salts were rinsed twice with dioxane. The mixture of the organic solutions was concentrated until an insoluble product appeared, and then poured over 400 ml of ice-cold water. The precipitate formed was drained, washed once with water and once with pentane. The brown powder obtained was dried under vacuum to a constant weight to give 16.8 g of N-(5-hydroxynaphthalen-1-yl)acetamide with a yield of 76%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605124B1
Source datasetuspto-grants-2003_08
ORD IDord-55fcf9a0869941169b9bf0431bf74234
Source noteuspto-grants-2003_08