HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → 2,6-Diisopropyl-4-(4-fluorophenyl)-3-hydroxymethyl-5-methoxyiminomethyl-pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 3-(tert.-Butyldimethylsilyloxymethyl)-2,6-diisopropyl-4-(4-fluorophenyl)5-methoxyiminomethyl-pyridine | HCID 137331182 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,6-Diisopropyl-4-(4-fluorophenyl)-3-hydroxymethyl-5-methoxyiminomethyl-pyridine | HCID 54462879 | — |
Reaction Steps
3.3 ml (3.3 mmol) of 1 M tetrabutylammonium fluoride solution in tetrahydrofuran is added to a solution of 1.5 g (3.3 mmol) of the compound from Example 1 in 15 ml of absolute tetrahydrofuran and the mixture is stirred at room temperature for 1 hour. Saturated sodium hydrogencarbonate solution is then added to the reaction solution and it is extracted several times with methylene chloride. The combined organic phases are dried (MgSO4), concentrated and then filtered through silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05064841 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-cb1b702f6efc4b509beff7f55f328f76 |
| Source note | uspto-grants-1991_11 |