HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromopropane → 6-(3-Bromopropoxy)-4-piperidino-2,3-dihydrobenzopyran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6-Hydroxy-4-piperidino-2,3-dihydrobenzopyran | HCID 13712848 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 6-(3-Bromopropoxy)-4-piperidino-2,3-dihydrobenzopyran | HCID 13712849 | — |
Reaction Steps
Crushed potassium hydroxide (1.15 g) and tetrabutyl ammonium chloride (0.61 g) are added to a solution of the product obtained in Step 3. (4.8 g) in 1,3-dibromopropane (21 ml). The reaction mixture is stirred under nitrogen at RT for 48 hours, diluted with diethyl ether, washed with water and extracted into 5% aq. HCl. The aqueous solution is washed with ether and made alkaline yielding a yellow oil which is taken up in ether, washed, dried, filtered and evaporated to give the desired product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04777168 |
| Source dataset | uspto-grants-1988_10 |
| ORD ID | ord-95b8a8006132494983a856a17648bc51 |
| Source note | uspto-grants-1988_10 |