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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082633Generated: October 30, 2026

Sulfuric Acid → (2-Methylbutyl)benzene

https://huagongshe.com/reaction/2082633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantBromobenzeneHCID 7961—
Reactant1-Butanol, 2-methyl-, 1-(4-methylbenzenesulfonate)HCID 301199—
SolventDiethyl EtherHCID 3283—
Product(2-Methylbutyl)benzeneHCID 10720364.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04082428
Source datasetuspto-grants-1978_04
ORD IDord-e6a52b362f0e44308be25e2d6078415c
Source noteuspto-grants-1978_04