HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dimethoxy-p-benzoquinone → Lonapalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dimethoxy-p-benzoquinone | HCID 76565 | — |
| Reactant | 3-Chloro-1-methoxybuta-1,3-diene | HCID 54290106 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Lonapalene | HCID 56237 | 117.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04933489 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-0532a38e91ac40a2b00d5333200d15a6 |
| Source note | uspto-grants-1990_06 |