HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium Fluoride → (1-Benzylpiperidin-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 1-Benzyl-2-(tert-butyldimethylsilyloxymethyl)piperidine | HCID 19891976 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1-Benzylpiperidin-2-yl)methanol | HCID 2735486 | 62.4% |
Reaction Steps
To an ice-cooled THF solution of tetrabutylammonium fluoride (1M, 3.2 ml) was dropwise added a THF (2 ml) solution of 1-benzyl-2-(tert-butyldimethylsilyloxymethyl)-piperidine (1.00 g, 3.2 mmol). After stirring at room temperature for 2 hours, a reaction solution was poured onto water followed by extraction with ethyl acetate (30 ml). The extract was washed successively with water and saturated aqueous sodium chloride and then dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure. The crude product thus obtained was purified by a column chromatography on silica gel (SiO2 : 20 g, CHCl3) to afford 0.41 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05124324 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-51054db7224a4378b2d663af651870ed |
| Source note | uspto-grants-1992_06 |