HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → [2-(Benzhydrylidene-amino)-3-fluoropyridin-4-yl]-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | Benzhydrylidene-[4-(tert-butyldimethylsilyloxymethyl)-3-fluoropyridin-2-yl]-amine | HCID 59139248 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2-(Benzhydrylidene-amino)-3-fluoropyridin-4-yl]-methanol | HCID 59139234 | — |
Reaction Steps
A mixture of benzhydrylidene-[4-(tert-butyldimethylsilyloxymethyl)-3-fluoropyridin-2-yl]-amine (14 mg, 32 μmol) and tetrabutylammonium fluoride (1 mol/L in THF) (65 μL, 65 μmol) in THF (0.5 mL) was stirred at room temperature for 30 minutes. Ethyl acetate was then added to the reaction solution, and the solution was washed with sodium hydrogen carbonate solution and saturated saline. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was distilled away under reduced pressure. The resultant residue was purified by silica gel column chromatography to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08569378B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-09a60985dfd949358b985696418b7540 |
| Source note | uspto-grants-2013_10 |