HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 8-[(4-Bromophenyl)methyl]-8-azabicyclo[3.2.1]octan-3-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 8-(4-Bromobenzyl)-8-aza-bicyclo[3.2.1]octan-3-one | HCID 55106469 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 8-[(4-Bromophenyl)methyl]-8-azabicyclo[3.2.1]octan-3-ol | HCID 58266833 | 90% |
Reaction Steps
Sodium borohydride (95 mg, 1.50 mmol) was added to a solution of 8-(4-bromobenzyl)-8-azabicyclo-[3.2.1]octan-3-one (0.22 g, 0.75 mmol) in methanol (10 mL) and the reaction mixture was stirred for 30 minutes. The reaction was diluted with water (10 mL) and extracted into DCM (3×20 mL). The combined organic layer was washed with saturated aqueous sodium bicarbonate solution (10 mL), dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to afford the title compound as an off-white solid (200 mg, 90%). 1H NMR (CDCl3, 300 MHz): 7.43 (dd, J=8.3, 2.0 Hz, 3H), 7.29-7.23 (m, 2H), 3.60-3.45 (m, 2H), 3.23-3.10 (m, 2H), 2.16-1.40 (m, 8H). LCMS (Method B): RT=1.90 min, M+H+=296/298.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08501765B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-6adca4a476cc4e1ebc5b4e81b1b03cdc |
| Source note | uspto-grants-2013_08 |