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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1082016Erstellt: 24. Oktober 2026

4-Toluenesulfonyl chloride → 4,4-Dimethyl-2-(4'-p-toluenesulfonyloxymethylbiphenyl-2-yl)oxazoline

https://huagongshe.com/de/reaction/1082016

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Toluenesulfonyl chlorideHCID 7397—
EduktSodium hydrideHCID 24758—
EduktAmmonium ChlorideHCID 25517—
Edukt4,4-Dimethyl-2-(4'hydroxymethylbiphenyl-2-yl)oxazolineHCID 11065876—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4,4-Dimethyl-2-(4'-p-toluenesulfonyloxymethylbiphenyl-2-yl)oxazolineHCID 1538087955%

Reaktionsschritte

0.34 g (8.5 mmol) of a 60% oily sodium hydride was suspended in tetrahydrofuran (20 ml). A solution of 2.0 g (7.1 mmol) of 4,4-dimethyl-2-(4'-hydroxymethylbiphenyl-2-yl)oxazoline in tetrahydrofuran (30 ml) was dropwise added thereto at room temperature, followed by further stirring at room temperature for one hour. After the reaction liquid was cooled with ice, a solution of 1.6 g (8.4 mmol) of p-toluenesulfonyl chloride in tetrahydrofuran (20 ml) was dropwise added thereto. After stirring for 3 hours as such, the reaction liquid was poured into a saturated aqueous solution of ammonium chloride, followed by the extraction with chloroform. After washing with water and drying, vacuum concentration was conducted. The residue was purified by silica gel column chromatography (a n-hexane/ethyl acetate system) to give 1.7 g of the title compound as an oil (yield 55%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05587504
Quelldatensatzuspto-grants-1996_12
ORD IDord-920aeca25ff242dba6678a534782d2b5
Quellennotizuspto-grants-1996_12