HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Bromo-7-methylphenanthrene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Bromo-7-methyl-phenanthrene-9-carboxylic acid | HCID 15159135 | — |
| Catalyst | HCID 10922056 | HCID 10922056 | — |
| Solvent | Quinoline | HCID 7047 | — |
| Solvent | Toluene methylene chloride | HCID 21877217 | — |
| Product | 3-Bromo-7-methylphenanthrene | HCID 15159136 | 103.1% |
Reaction Steps
A stirred mixture of 3-Bromo-7-methyl-phenanthrene-9-carboxylic acid (5.50 g, 17.5 mmol) and CuCo3.Cu(OH)2.H2O (1.5 g) in 50 ml of quinoline was rapidly heated to 210° C. Gas evolution was observed and the mixture became extremely dark. After 10 min the mixture was allowed to cool to room temperature and was diluted with PhCH3 --CH2Cl2 (9:1) and filtered. The filtrate was washed with 1N HCl (2x) and brine. Drying (Na2SO4) and evaporation gave 4.89 g of a brown oil which was flash chromatographed through 450 g of silica gel (10% CH2Cl2 /hexane) to yield 2.63 g (56%) of the title compound as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05196529 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-9183f5bb19c247f1898ab45227e6c85a |
| Source note | uspto-grants-1993_03 |