HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 76851486, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 21979982 | HCID 21979982 | — |
| Catalyst | HCID 178527703 | HCID 178527703 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 76851486 | HCID 76851486 | 102.1% |
Reaction Steps
A solution of 4-bromo-1-chloro-5-nitroisoquinoline (14.0 g) prepared according to the method described in a known literature (Nair et al., Indian J. Chem., 1967, 5, 403) in ethanol (75 ml) and tetrahydrofuran (75 ml) was added with 3% platinum-sulfur/activated carbon (3% Pt—S/C, NE Chemcat, CM101, 14.0 g), and the mixture was stirred at room temperature for 15 hours under a hydrogen gas atmosphere. The atmosphere was replaced with nitrogen gas, and then the insoluble solids were removed by filtration through Celite, and the solvent was evaporated under reduced pressure to obtain the title compound (12.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07964613B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-8bf5af9bd68242f9a488e269d83b3ad2 |
| Source note | uspto-grants-2011_06 |