HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → HCID 20289175, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Chlorobenzyl alcohol | HCID 13397 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Product | HCID 20289175 | HCID 20289175 | — |
Reaction Steps
To a solution of 1-chloro-4-hydroxymethylbenzene (14.2 g, 0.1 mol) in tetrahydrofuran (250 ml) was added sodium hydride as a 40% suspension in oil (4 g, 0.1 mol) portionwise under nitrogen. When effervescence ceased iodoethane (15.6 g, 0.1 mol) was added and the solution heated at reflux for 8 hours. The reaction was quenched with water and extracted with ethyl acetate. The organic layer was washed with dilute aqueous sodium hydroxide and brine, then dried (MgSO4) and evaporated to dryness. The subtitle compound was obtained as a clear oil (17.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06306852B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-5eb42fee362b4d488497b5d7f3ea7942 |
| Source note | uspto-grants-2001_10 |