HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,6-Dibromohexane → HCID 23045257, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,6-Dibromohexane | HCID 12368 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-{[2-(2-Pyridinyl)ethyl]thio}ethanol | HCID 23422527 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 23045257 | HCID 23045257 | 63.5% |
Reaction Steps
A mixture of 2-[[2-(2-pyridinyl)ethyl]thio]ethanol (0.50 g), 1,6-dibromohexane (2.13 g), TAB (0.4 g) and 50% aqueous sodium hydroxide (6 ml) was stirred under nitrogen for 6 h, then diluted with water (75 ml) and extracted with diethyl ether (2×150 ml). The organic extracts were evaporated in vacuo to give an oil, which was partitioned between 2N hydrochloric acid (100 ml) and hexane (2×100 ml). The aqueous phase was basified to pH 12 with 50% aqueous sodium hydroxide and extracted with diethyl ether (2×150 ml), the dried organic extracts were evaporated in vacuo to give an oil. Purification by FCC eluting with System F (1:1) gave the title compound (0.60 g) as a colourless oil. T.l.c. (diethyl ether) Rf 0.64
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04937268 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-4a20ad5028044648ab25d1acb0dbc34c |
| Source note | uspto-grants-1990_06 |