HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → tert-Butyl (6-bromo-1,2,3,4-tetrahydroquinolin-3-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Boc-3-amino-1,2,3,4-tetrahydroquinoline | HCID 4460996 | — |
| Reactant | Pyridiniumtribromide | HCID 21124087 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl (6-bromo-1,2,3,4-tetrahydroquinolin-3-yl)carbamate | HCID 17758659 | 1,863.5% |
Reaction Steps
To a solution of 1A (2.7 g, 10.9 mmol) in THF (50 mL) at RT was added dropwise a solution of pyridinium tribromide (3.83 g, 0.41 mmol) in THF (50 mL). After addition, the reaction mixture was stirred for 15 min, then water (60 mL) and ether (60 mL) added. The aqueous layer was separated, and extracted with EtOAc (2×50 mL). The combined organics were washed with brine, dried (Na2SO4) and concentrated. The residue was chromatographed (silica gel) eluting with EtOAc (0 to 50%) in hexane to give the title compound (2.5 g, 70% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07884113B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-d45b58b72ad84b7aa70b7374ab0c3a26 |
| Source note | uspto-grants-2011_02 |