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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107350Generated: October 30, 2026

2,3-Dimethoxy-p-benzoquinone → Lonapalene

https://huagongshe.com/reaction/2107350

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dimethoxy-p-benzoquinoneHCID 76565—
Reactant3-Chloro-1-methoxybuta-1,3-dieneHCID 54290106—
SolventDichloromethaneHCID 6344—
ProductLonapaleneHCID 56237117.1%

Reaction Steps

A dichloromethane (10 ml) solution of 2,3-dimethoxybenzo-1,4-quinone (1.0 g, 5.9 mmol) and 3-chloro-1-methoxy-1,3-butadiene (1.4 g, 12.0 mmol) is stirred for 24 hours at room temperature under an inert atmosphere. After this time, 80 mg of d,1-camphorsulfonic acid is added and the solution is stirred an additional 12 hours. The mixture is then concentrated and subsequently dissolved in pyridine (15 ml) and acetic anhydride (3.0 g). After stirring for five hours under an inert atmosphere, the solution is concentrated to dryness and taken up in dichloromethane. The organics are washed with water, brine, and then dried (sodium sulfate) and concentrated to afford 1.17 g (58%) of pure 6-chloro-1,4-diacetoxy-2,3-dimethoxynaphthalene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04933489
Source datasetuspto-grants-1990_06
ORD IDord-0532a38e91ac40a2b00d5333200d15a6
Source noteuspto-grants-1990_06