HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium Fluoride → 2-Phenyl-1,3-dioxolane-2-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 68160183 | HCID 68160183 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Phenyl-1,3-dioxolane-2-methanol | HCID 12614248 | 45.5% |
Reaction Steps
To a solution of tert-butyldimethyl-(2-phenyl-[1,3]dioxolan-2-yl-methoxy)silane (5.5 g, 18.7 mmol) in tetrahydrofuran (50 ml) was added tetrabutylammonium fluoride (1M in tetrahydrofuran, 56 ml) at room temperature. The mixture was stirred at room temperature for 12 hours. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent; hexane/ethyl acetate=3/1) to give (2-phenyl-[1,3]dioxolan-2-yl)methanol (1.54 g, 8.5 mmol, 45%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09006232B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-98d9baa0ab004de2880df39a0a1feb61 |
| Source note | uspto-grants-2015_04 |