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 | Benzene | HCID 241 | — |
| Product | Lonapalene | HCID 56237 | 203.1% |
Reaction Steps
A benzene (8 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 30 hours under an inert atmosphere. After this time, the reaction mixture is concentrated and then dissolved in pyridine (8 ml). Acetic anhydride (3.0 g) is added, and the solution is stirred for 12 hours under an inert atmosphere. The contents are diluted ten-fold with water and extracted with ethyl acetate. The organics are then washed with water, brine, and then dried over sodium sulfate. Concentration, followed by flash chromatography (hexane/ethyl acetate 3:1) affords 2.03 g (93%) of a compound of the formula ##STR5##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04933489 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-248cfa3ba8a0455b8a56b6ab461caaa2 |
| Source note | uspto-grants-1990_06 |