HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromopropane → 4-(3-Bromopropoxy)-2,2-dimethyl-1-(1-piperidinyl)indan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 20137132 | HCID 20137132 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(3-Bromopropoxy)-2,2-dimethyl-1-(1-piperidinyl)indan | HCID 20137130 | — |
Reaction Steps
Potassium hydroxide (1.44 g) is added to a stirred solution of the 4-hydroxy compound of Step 4. above (5 g) in methylene chloride (44 ml) and stirring is continued under N2 for 30 min. 1,3-Dibromopropane (20.7 ml) and tetrabutyl ammonium chloride (0.63 g) are added and the mixture is stirred at RT for about 70 hours. The reaction mixture is diluted with methylene chloride, washed with H2O, dried, filtered and the filtrate evaporated in vacuo. The residue is chromatographed (silica gel, hexane/ether) affording the purified desired product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04588719 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-04d9ad36cfa0474889b6ec750ae5646c |
| Source note | uspto-grants-1986_05 |