HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → (S)-2-(5-bromo-2,7-dimethylquinolin-6-yl)-2-tert-butoxyethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (S)-2-(5-bromo-2,7-dimethylquinolin-6-yl)-2-tert-butoxyethyl pivalate | HCID 66630692 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-2-(5-bromo-2,7-dimethylquinolin-6-yl)-2-tert-butoxyethanol | HCID 66631978 | — |
Reaction Steps
To a stirred solution of (S)-2-(5-bromo-2,7-dimethylquinolin-6-yl)-2-tert-butoxyethyl pivalate (50.0 g, 115 mmol) in THF (600 mL) and methanol (200 mL) was added 1M NaOH solution (300 mL, excess) at 0° C. The mixture was stirred at room temperature for 16 hours, diluted with water. The mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried and concentrated in vacuo. The obtained residue was purified by flash chromatography to provide the desired product. LCMS-ESI+: calc'd for C17H22BrNO2: 352.1 (M+H+); Found: 352.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09376392B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-c4517cced6a442d18b32c5dc0e937a4f |
| Source note | uspto-grants-2016_06 |