HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Hexyne → HCID 178442536, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Hexyne | HCID 12732 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178444300 | HCID 178444300 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 178442536 | HCID 178442536 | — |
Reaction Steps
10 ml of a 20% solution of diisobutylaluminium hydride in hexane are added to a solution of 0.01 mol of 1-hexyne and 5 ml of hexane and the mixture is heated at 50° for 3 hours. It is then cooled to 25°, 6.3 ml of a 15% solution of butyllithium in hexane are added dropwise, after 30 minutes 0.01 mol of 2,3-difluoro-4-(trans-4-pentylcyclohexyl)-methoxybenzyl bromide, dissolved in 15 ml of tetrahydrofuran, are added dropwise and the mixture is heated under reflux for 12 hours. Working up gives 2,3-difluoro-4-(trans-4-pentylcyclohexyl)-methoxy-trans-hept-2-enylbenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05279764 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-0ad5fd52a0814aa69ebdc3b27e28e809 |
| Source note | uspto-grants-1994_01 |