Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Product | (2-Methylbutyl)benzene | HCID 107203 | — |
Reaction Steps
A phenylmagnesium bromide solution prepared from 40 g of bromobenzene, 6.2 g of magnesium and 300 ml of ether was cooled at 5° C., and a mixture liquid of 125 g of 2'-methylbutyl 4-methylbenzenesulfonate (II) prepared above and 130 ml of ether was added dropwise. After 2 hours of stirring, the mixture was elevated in temperature to effect 2 hours of refluxing, followed by standing overnight. To the reaction liquid, 10 % H2SO4 was added with pH 2. The organic layer was washed successivly with an aqueous sodium bicarbonate solution and water, followed by drying with anhydrous magnesium sulfate, and distilling-off of the solvent. The product was distilled under reduced pressure to obtain 48 g of 4-(2'-methylbutyl)benzene (III), which showed the following IR data:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04816178 |
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| Source dataset | uspto-grants-1989_03 |
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| ORD ID | ord-fce69c9f463a4f9e9b0e547ee0e77066 |
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| Source note | uspto-grants-1989_03 |
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