HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromonaphthalene → 1,1-Diethoxy-1,2-dihydrocyclobuta[a]naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromonaphthalene | HCID 7001 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | 1,1-Diethoxyethene | HCID 137673 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1,1-Diethoxy-1,2-dihydrocyclobuta[a]naphthalene | HCID 18467793 | — |
Reaction Steps
9.4 g of sodium amide are introduced into 350 ml of tetrahydrofuran. 25.9 g of 1-bromonaphthalene and 28 g of freshly prepared 1,1-diethoxyethylene are poured in succession into that mixture. The reaction mixture is refluxed for 16 hours and than taken up in water and ether. After washing the organic phase to neutral pH and drying thereof, the expected product is isolated and chromatographed over silica gel (dichloromethane/cyclohexane: 1/1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06420413B2 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-1b0510dcb64a474a98ea830319b4c1d8 |
| Source note | uspto-grants-2002_07 |