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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1645702Erstellt: 24. Oktober 2026

2-Methyl-2-butanol → Heptylbenzene

https://huagongshe.com/de/reaction/1645702

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Methyl-2-butanolHCID 6405—
Edukt1-BromoheptaneHCID 12369—
EduktPhenylboronic AcidHCID 66827—
EduktDi-tert-butyl(methyl)phosphanium tetraphenylborate(1-)HCID 23136641—
EduktPotassium tert-butoxideHCID 23665647—
Katalysatorpalladium(II) acetateHCID 167845—
ProduktHeptylbenzeneHCID 1411589,1%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08124809B2
Quelldatensatzuspto-grants-2012_02
ORD IDord-2e2d0db01e774cce85bfef4ec6c5ac44
Quellennotizuspto-grants-2012_02