HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Butanol → 6,6'-Dimethyl-2'-n-butoxy-2,3',4'-trimethoxy-benzophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6,6'-Dimethyl-2,2',3',4'-tetramethoxy-benzophenone | HCID 15431060 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6,6'-Dimethyl-2'-n-butoxy-2,3',4'-trimethoxy-benzophenone | HCID 15870895 | — |
Reaction Steps
A mixture of n-butanol (5 ml) and sodium hydride (60% in oil, 10 mmol) is stirred until the formation of H2 gas ceases. A mixture of 1C (0.7 g, 2.2 mmol) and dimethoxyethane (15 ml) is added to the resulting reaction mixture. Subsequently, the reaction mixture is heated under reflux with stirring for 24 hours. A mixture of water and ethyl acetate (1:1 v/v; 100 ml) is then slowly added at room temperature. The organic phase is separated, concentrated and the residue is purified by column chromatography (petrol ether:ethyl acetate, 95:5 v/v) yielding the pure product as a yellow oil, 0.2 g, (24.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06001883 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-7edf6c5fb39646c1a177b241bb6272f8 |
| Source note | uspto-grants-1999_12 |