HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Methyl-7-phenylnaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-Bromo-7-methylnaphthalene | HCID 15321336 | — |
| Reactant | HCID 178506676 | HCID 178506676 | — |
| Catalyst | HCID 178418745 | HCID 178418745 | — |
| Product | 2-Methyl-7-phenylnaphthalene | HCID 12353017 | — |
Reaction Steps
Solution of 2-bromo-7-methylnaphthalene (10 g, 45 mmole) in ether (100 ml) was cooled to −0° C., and Ni(dppp)Cl2 and solution of PhLi (obtained from 1.3 g of Mg and 5.6 ml of PhBr in 55 ml of ether) were added subsequently. Reaction mixture was allowed to warm to room temperature, stirred for additional 4 h with heating, cooled room temperature, stirred for additional 16 h, and treated by water (100 ml). Organic layer was separated, water layer was extracted by ether (3×50 ml). Combined organic fraction was evaporated, giving practically pure solid product. The yield 9.23 g (94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07579417B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-cebdd5ffeea74035981f44be2604aa61 |
| Source note | uspto-grants-2009_08 |