HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Oxide → 2,4-Bis(1,1-dimethylethyl)benzeneethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 1-Bromo-2,4-di-tert-butylbenzene | HCID 11076464 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,4-Bis(1,1-dimethylethyl)benzeneethanol | HCID 19936080 | — |
Reaction Steps
To 243 mg (10 mmoles) of magnesium turnings in 10 ml of tetrahydrofuran is added dropwise a solution of 2.69 grams (10 mmoles) of the title product of Example 9 in 5 ml of tetrahydrofuran. After the addition is complete, the mixture is refluxed for one hour. Ethylene oxide (440 mg, 10 mmoles) is then added, and refluxing continued for one hour. The mixture is cooled to room temperature and partitioned between saturated ammonium chloride and diethyl ether. The aqueous layer is further extracted with ether, the combined organic extracts washed with brine, dried over sodium sulfate, filtered, and evaporated. Chromatography of the residue over silica gel using mixtures of ethyl acetate and hexane as eluents gives the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05420343 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-4db0bebb53404ac29f05848985b87693 |
| Source note | uspto-grants-1995_05 |