HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dibromobutane → 7-(4-Bromobutoxy)-3-piperidino-2,2-dimethylbenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 7-Hydroxy-3-piperidino-2,2-dimethylbenzofuran | HCID 14126650 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 7-(4-Bromobutoxy)-3-piperidino-2,2-dimethylbenzofuran | HCID 21289001 | — |
Reaction Steps
Crushed potassium hydroxide (19.6 g) and tetrabutyl ammonium chloride (1.7 g) are added to a solution of 7-hydroxy-3-piperidino-2,2-dimethylbenzofuran (14.4 g) in 1,4-dibromobutane (69.4 ml) and the mixture stirred at RT under nitrogen for 5 hours. The reaction mixture is diluted with ether, washed with water, extracted with 5% aq. HCl and the acidic phase washed with ether. The acidic phase is made basic thereby forming an oil which is taken up in ether, washed with sat'd aq. NaCl, dried, filtered and evaporated in vacuo affording the desired product as a liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04722925 |
| Source dataset | uspto-grants-1988_02 |
| ORD ID | ord-e1cc7aae472c4f0e89601c6881976e37 |
| Source note | uspto-grants-1988_02 |