HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505941Generated: October 30, 2026
Triethylamine → 8-(4-Bromobenzyl)-8-aza-bicyclo[3.2.1]octan-3-one
https://huagongshe.com/reaction/1505941
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | 8-Azabicyclo(3.2.1)octan-3-one | HCID 434453 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-(4-Bromobenzyl)-8-aza-bicyclo[3.2.1]octan-3-one | HCID 55106469 | 90% |
Reaction Steps
A stirred solution of 1-bromo-4-bromomethylbenzene (0.39 g, 1.56 mmol), triethylamine (0.45 mL, 3.20 mmol) and 8-azabicyclo[3.2.1]octan-3-one (0.33 mL, 2.32 mmol) in THF (10 mL) was heated under reflux for 5 h. The reaction mixture was allowed to cool to ambient temperature and the solid removed by filtration. The filtrate was concentrated under reduced pressure to afford a residue that was purified by flash chromatography (silica, 50 g column, Biotage, 0-100% DCM in ethyl acetate) to afford the title compound as an off-white solid (400 mg, 90%). 1H NMR (CDCl3, 300 MHz): 7.48-7.43 (m, 2H), 7.32-7.28 (m, 2H), 3.69 (s, 2H), 3.49-3.43 (m, 2H), 2.66 (dd, J=16.0, 4.3 Hz, 2H), 2.26-2.17 (m, 2H), 2.14-2.06 (m, 2H), 1.66-1.56 (s, 2H). LCMS (Method B): RT=1.86 min, M+H+=294/296.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09216980B2 |
|---|
| Source dataset | uspto-grants-2015_12 |
|---|
| ORD ID | ord-935a50bbcd244d348a745a4a9f7a26c8 |
|---|
| Source note | uspto-grants-2015_12 |
|---|