HuagongsheHuagongshe Chemistry Print Report · For research reference only
Catechol → 3-Methylene-3,4-dihydro-2H-1,5-benzodioxepin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Catechol | HCID 289 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloro-2-chloromethyl-1-propene | HCID 15859 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Methylene-3,4-dihydro-2H-1,5-benzodioxepin | HCID 595450 | — |
Reaction Steps
Catechol (5.09 g, 46.2 mmol) and potassium carbonate were combined in acetonitrile and heated to reflux for one hour. 2-Chloromethyl-3-chloro-1-propene (5.78 g, 46.2 mmol) was added and the reaction was continued at reflux for 24 hours. The solution was cooled to room temperature and filtered. The filtrate was evaporated and the residue was diluted with water and extracted with diethyl ether (3×). The combined organic solution was dried over MgSO4 and concentrated. Chromatography (2% ethyl ether in hexane) yielded 3-methylene-3,4-dihydro-2H-benzo[b][1,4]dioxepine as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084490B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-52cbea49617b44faa83030e2bc163169 |
| Source note | uspto-grants-2011_12 |