Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13887Generated: October 25, 2026

2-Methyl-2-butanol → Heptylbenzene

https://huagongshe.com/reaction/13887

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 numberUS07728176B2
Source datasetuspto-grants-2010_06
ORD IDord-c25732fe82a044a998fee3f740d7f5f2
Source noteuspto-grants-2010_06