HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 4-Butyl-2-phenyl-1,3-dioxolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 1,2-Hexanediol | HCID 94335 | — |
| Catalyst | Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- | HCID 18462 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Butyl-2-phenyl-1,3-dioxolane | HCID 21710576 | 102.2% |
Reaction Steps
A solution of benzaldehyde (5.1 mL, 50.0 mmol), 1,2-hexanediol (6.5 g, 55.0 mmol), and camphorsulfonic acid (0.58 g, 2.5 mmol) in 50 mL of toluene was heated to reflux (Dean-Stark) with azeotropic removal of water. When the theoretical amount of water was distilled (4.5 hours), the mixture was cooled to room temperature and diluted with 80 mL of ether. The solution was extracted with 2M aqueous sodium carbonate, water and brine, dried (Na2SO4), filtered, and concentrated to provide 10.54 g (102%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06277871B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-50e9d02e287546d8aa1ddab3807cf092 |
| Source note | uspto-grants-2001_08 |