HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Bromo-1,2,3,4-tetrahydronaphthalen-1-one → HCID 18960968, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Bromo-1,2,3,4-tetrahydronaphthalen-1-one | HCID 252731 | — |
| Reactant | Sodium pentafluoropropionate | HCID 2733305 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 18960968 | HCID 18960968 | 80% |
Reaction Steps
To a solution of 10 g (0.044 mol) of 7-bromo-1,2,3,4-tetrahydronaphthalenone in 300 mL of N-methylpyrrolidone was added 32.23 g (0.17 mol) of CuI and 31.59 g (0.17 mol) of sodium pentafluoropropanoate and the mixture was heated for 3 h at reflux under an argon atmosphere. After cooling to room temperature, the resulting suspension was poured into a mixture of H2O--Et2O (1:1) and filtered over celite. The layers were separated and the organic phase was washed with H2O and dried over MgSO4. The solvent was removed, to afford a residue that was chromatographed on silica gel (hexane-AcOEt), to give the desired product as a colourless oil (8.75 g, yield: 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05356915 |
| Source dataset | uspto-grants-1994_10 |
| ORD ID | ord-aa0504312d864e5b9b58d58be25e9cb3 |
| Source note | uspto-grants-1994_10 |