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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 53267Erstellt: 24. Oktober 2026

p-Toluenesulfonic acid → t-Butylphenol 2-Phenyl-2-oxazoline

https://huagongshe.com/de/reaction/53267

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Toluenesulfonic acidHCID 6101—
Edukt2-Tert-ButylphenolHCID 6923—
Edukt2-Phenyl-2-oxazolineHCID 244030—
LösungsmittelTetrahydrofuranHCID 8028—
Produktt-Butylphenol 2-Phenyl-2-oxazolineHCID 86750688—

Reaktionsbedingungen

Temperatur170 °C

Reaktionsschritte

A pure sample of the addition product of t-butylphenol and 2-phenyl-2-oxazoline was obtained for comparative purposes as follows: in a side-armed test tube, 2.94 grams 2-phenyl-2-oxazoline and 3.00 grams t-butyl phenol were combined with 0.08 gram pTSA. The stirred mixture was heated under nitrogen at 170° C. for 16 hours. Pure amide ether addition product [B] was obtained from the reaction mixture by column chromatography on silica gel. The crude reaction mixture was taken up in tetrahydrofuran and introduced onto the column, which was subsequently eluted with 1/1 (v/v) hexane/ethyl acetate. Desired fractions were identified by thin layer chromatography, and the product structure was confirmed by 1H and 13C NMR. The reaction is outlined in Scheme 1. ##STR3##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05618896
Quelldatensatzuspto-grants-1997_04
ORD IDord-6b81bcb965514342b8020cef002faef9
Quellennotizuspto-grants-1997_04