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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645702Generated: October 26, 2026

2-Methyl-2-butanol → Heptylbenzene

https://huagongshe.com/reaction/1645702

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-butanolHCID 6405—
Reactant1-BromoheptaneHCID 12369—
ReactantPhenylboronic AcidHCID 66827—
ReactantDi-tert-butyl(methyl)phosphanium tetraphenylborate(1-)HCID 23136641—
ReactantPotassium tert-butoxideHCID 23665647—
Catalystpalladium(II) acetateHCID 167845—
ProductHeptylbenzeneHCID 1411589.1%

Reaction Steps

A 50-ml four-necked flask was equipped with a stirrer, a thermometer and a reflux condenser. 0.896 g (5 mmol) of n-heptyl bromide, 0.914 g (7.5 mmol) of phenylboronic acid, 0.056 g (0.25 mmol) of palladium (II) acetate, 1.683 g (15 mmol) of potassium tert-butoxide and 25 ml of tert-amyl alcohol were weighed in the flask, followed by stirring. Further, 0.240 g (0.5 mmol) of di-tert-butylmethylphosphonium tetraphenylborate obtained in Example B-1 was weighed in air and added into the flask. The flask was purged with argon, followed by stirring at 25° C. for 24 hours. After the completion of the reaction, 20 ml of saturated sodium chloride solution was added, followed by separation. The organic phase was purified by column chromatography to afford 0.785 g of 1-phenylheptane (yield: 89 mol % based on n-heptyl bromide). The identification of the product was made by mass spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124809B2
Source datasetuspto-grants-2012_02
ORD IDord-2e2d0db01e774cce85bfef4ec6c5ac44
Source noteuspto-grants-2012_02