Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | 1-Butanol, 2-methyl-, 1-(4-methylbenzenesulfonate) | HCID 301199 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (2-Methylbutyl)benzene | HCID 107203 | 64.8% |
Reaction Steps
Phenylmagnesium bromide-ether solution was prepared from bromobenzene (64.5g, 0.41m), magnesium turnings (9.85g, 0.41m), and anhydrous ether (500ml). The reagent was cooled and (+)-β-methylbutyl-4-toluenesulfonate (200g, 0.82m) in ether (800ml) was added in drops. When the addition was complete, the reaction mixture was stirred for two hours, refluxed for two hours and left to stand overnight. Aqueous sulfuric acid was added until a clear solution was formed. The layers were separated. The aqueous layer was extracted with ether (3×250ml), and the combined organic layers were washed with sodium bicarbonate solution, water and dried over anhydrous sodium sulfate. The solvent was evaporated and the residue was steam-distilled. Fractional distillation of the crude product at reduced pressure yielded (+)-β-methylbutylbenzene (38.7g, 64.8%), bp. 74°-77° C at 12 mm pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04082428 |
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| Source dataset | uspto-grants-1978_04 |
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| ORD ID | ord-e6a52b362f0e44308be25e2d6078415c |
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| Source note | uspto-grants-1978_04 |
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