HuagongsheHuagongshe Chemistry Print Report · For research reference only
Catechol → Spiro[1,3-benzodioxole-2,1′-cyclopentane]
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Catechol | HCID 289 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Cyclopentanone | HCID 8452 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Spiro[1,3-benzodioxole-2,1′-cyclopentane] | HCID 12608169 | — |
Reaction Steps
Catechol (11 g) and cyclopentanone (9 ml) were heated under reflux in toluene (150 ml) with p-toluenesulfonic acid (0.18 g) with a water trap. After 18 hours, the mixture was concentrated and purified by chromatography (silica gel, heptane/ethyl acetate 4:1). This resulted in the product with the molecular weight of 176.22 (C11H12O2); MS(ESI): 177 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07223788B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-289e1de8b3384f3fb86d5f070da8e726 |
| Source note | uspto-grants-2007_05 |