HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,6-Dibromohexane → 2-[3-[(6-Bromohexyl)oxy]propyl]thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,6-Dibromohexane | HCID 12368 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-(Thiophen-2-yl)propan-1-ol | HCID 13109866 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[3-[(6-Bromohexyl)oxy]propyl]thiophene | HCID 19996103 | 61.5% |
Reaction Steps
A mixture of 2-thiphenepropanol (5 g), 1,6-dibromohexane (25 g), 50% aqueous sodium hydroxide (25 ml) and TAB (500 mg) was stirred at room temperature overnight. Water (100 ml) was added over and the mixture was extracted with ether (2×100 ml). The organic layer was dried and concentrated to an oil which was purified by FCC eluting with hexane to give the title compound as a colourless oil (6.6 g). T.l.c. (hexane-diethyl ester 9:1) Rf 0.50.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05032609 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-1f61b55ea6764fe0bf4c543610b6106a |
| Source note | uspto-grants-1991_07 |