Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442429Generated: October 30, 2026

Acetyl chloride → 1-(5-Chloro-6-methoxynaphthalen-2-yl)ethan-1-one

https://huagongshe.com/reaction/442429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant1-Chloro-2-methoxynaphthaleneHCID 11564623—
SolventNitrobenzeneHCID 7416—
Product1-(5-Chloro-6-methoxynaphthalen-2-yl)ethan-1-oneHCID 15890459—

Reaction Steps

A mixture of 1925 g. of 1-chloro-2-methoxynaphthalene, 80 g. of acetyl chloride, 400 g. of aluminum chloride and 2.5 liters of nitrobenzene are stirred for 60 hours at room temperature. The temperature mixture is then washed with dilute hydrochloric acid, dried over sodium sulfate and evaporated to yield 2-acetyl-5-chloro-6-methoxynaphthalene. The resulting acetyl product is added to a mixture of 39 g. of sulfur and 105 g. of morpholine and heated to about 150° C for 3 hours. The mixture is then added to 1 liter of concentrated hydrochloric acid and refluxed for 3 hours. The mixture is then cooled, diluted with 6 liters of ice-water and extracted with methylene chloride. The extracts are combined, washed with water to neutrality, dried over sodium sulfate and evaporated to yield 2-(5'-chloro-6'-methoxy-2'-naphthyl) acetic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04045485
Source datasetuspto-grants-1977_08
ORD IDord-100bab4a8e1d495a84d051b48ca3bbf9
Source noteuspto-grants-1977_08