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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566975Generated: October 25, 2026

2-Methoxynaphthalene → 3-Methoxyacenaphthoquinone

https://huagongshe.com/reaction/566975

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxynaphthaleneHCID 7119—
ReactantOxalyl chlorideHCID 65578—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantDry ice ethyleneglycolHCID 86601574—
SolventDichloromethaneHCID 6344—
Product3-MethoxyacenaphthoquinoneHCID 225026467.1%

Reaction Steps

A solution of 2-methoxynaphthalene (5 g, 31.6 mmol) and oxalyl chloride (11 mL, 126 mmol) in 150 mL of dichloromethane was cooled to −15° C. (CO2/ethylene glycol) under nitrogen. Aluminum trichloride (10.5 g, 79 mmol) was added slowly over 30 minutes. After 3 hours, the mixture was poured onto 100 g of ice. The layers were separated, and the aqueous layer was washed with dichloromethane. The combined organic layers were washed with saturated sodium bicarbonate, water, brine and dried over magnesium sulfate. The solution was concentrated to afford 4.5 g of a solid. The solid was triturated with dichloromethane to give 1.24 g of the title compound as a solid, mp 218°-220° C.; 1H NMR (DMSO-d6): δ8.38 (d, 1H), 8.25 (d, 1H), 7.90 (d, 1H), 7.63 (m, 2H), 4.07 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177423B1
Source datasetuspto-grants-2001_01
ORD IDord-3a13157bbb5f4060a050e2da0fa024e0
Source noteuspto-grants-2001_01