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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13887Erstellt: 24. Oktober 2026

2-Methyl-2-butanol → Heptylbenzene

https://huagongshe.com/de/reaction/13887

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
PatentnummerUS07728176B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-c25732fe82a044a998fee3f740d7f5f2
Quellennotizuspto-grants-2010_06