HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 2-[2-[(6-Bromohexyl)oxy]ethyl]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 1,6-Dibromohexane | HCID 12368 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Quinolineethanol | HCID 70532 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-[2-[(6-Bromohexyl)oxy]ethyl]quinoline | HCID 22161749 | — |
Reaction Steps
A mixture of 2-quinolineethanol (1.00 g), 1,6-dibromohexane (4 ml), TAB (100 mg), 50% aqueous sodium hydroxide (4 ml) and dichloromethane (3 ml) was stirred at room temperature for 40 h, then diluted with water (40 ml) and ether (25 ml). The organic phase was washed with water (20 ml), dried and evaporated in vacuo. The residual oil was purified by FCC eluting with hexane followed by hexane-ether (9:1) and ether, to give the title compound (1.18 g) as a pale yellow oil, t.l.c. (diethyl ether) Rf 0.44.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04963564 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-7431bd3e640a4eb8959f2b7909f12814 |
| Source note | uspto-grants-1990_10 |