HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Ethylphenol → 1-(4-Bromobutoxy)-2-ethylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Ethylphenol | HCID 6997 | — |
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Product | 1-(4-Bromobutoxy)-2-ethylbenzene | HCID 43364277 | — |
Reaction Steps
The solution of 19.04 ml of 2-ethylphenol in 24 ml of 1,4-dibromobutane is heated to 100° C. with stirring and admixed slowly with 99.2 ml of 1.6M NaOH. The emulsion is stirred at 100° C. over 20 h. The reaction mixture is cooled and extracted with tert-butyl methyl ether (2×150 ml). The organic phases are washed successively with 2M NaOH (1×150 ml), water (1×150 ml) and brine (1×150 ml), dried over sodium sulphate, filtered and concentrated by evaporation. The title compound is obtained as a slightly yellowish oil from the residue by means of distillation. b.p. 132° C. (1.1 mbar); Rt=5.75.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07842688B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-80a614fcc0b642a8b97dd7ed8ab2e122 |
| Source note | uspto-grants-2010_11 |