HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-n-Butyl-3-[4-(N-t-butyl-3-azetidinoxy)benzoyl]benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (2-Butylbenzofuran-3-yl) (4-hydroxyphenyl) ketone | HCID 96670 | — |
| Reactant | 1-(Tert-butyl)-3-chloroazetidine | HCID 10997186 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-n-Butyl-3-[4-(N-t-butyl-3-azetidinoxy)benzoyl]benzofuran | HCID 21510506 | — |
Reaction Steps
A mixture of 3.98 g. (13.5 mmol.) of 2-n-butyl-3-(4-hydroxybenzoyl)benzofuran, 2.0 g. (13.5 mmol.) of N-t-butyl-3-chloroazetidine and 0.54 g. of sodium hydroxide in 75 ml. of ethanol was refluxed for five hours. The reaction mixture was cooled, filtered and 125 ml. of 10% aqueous sodium hydroxide solution was added. The mixture was extracted three times with chloroform, the combined extracts were evaporated to dryness and the residue was chromatographed on alumina with chloroform as eluant to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03983245 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-ef9d1bc1a75f481eaf7729a0fb778372 |
| Source note | uspto-grants-1976_09 |