HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505044Generated: October 26, 2026
Cesium fluoride → 5-Bromo-2-(2,2-difluoropropyl)-1,2,3,4-tetrahydroisoquinoline
https://huagongshe.com/reaction/1505044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(5-Bromo-3,4-dihydroisoquinolin-2(1H)-yl)propan-2-one | HCID 58318043 | — |
| Catalyst | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromo-2-(2,2-difluoropropyl)-1,2,3,4-tetrahydroisoquinoline | HCID 58317935 | — |
Reaction Steps
To a solution of 1-(5-bromo-3,4-dihydroisoquinolin-2(1H)-yl)propan-2-one (962 mg, 3.59 mmol), diethylamino sulfur trifluoride (1.74 g, 10.8 ml) in DCM (12 ml) is added cesium fluoride (151 mg, 1 mmol) in small portions, then a few drops of TFA at room temperature. The mixture is stirred for 18 hours at room temperature. To this solution is added saturated aqueous NaHCO3 to quench the reaction. The aqueous layer is extracted with DCM (50 ml×3). The combined organic layers are washed with water, brine, dried over MgSO4 and concentrated. The residue is purified by silica gel flash chromatography, eluted with 20% ethyl acetate in hexanes to yield 5-Bromo-2-(2,2-difluoropropyl)-1,2,3,4-tetrahydroisoquinoline as a brown oil. LC-MS m/z: 291.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09216964B2 |
|---|
| Source dataset | uspto-grants-2015_12 |
|---|
| ORD ID | ord-47a4b8a206f54694879b129ae950a696 |
|---|
| Source note | uspto-grants-2015_12 |
|---|