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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1606329Erstellt: 25. Oktober 2026

Acetic Anhydride → 6,8-di-t-butyl-4-oxo-4H-1-benzopyran-2-carboxylic acid, ethyl ester

https://huagongshe.com/reaction/1606329

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
EduktSodium BicarbonateHCID 516892—
EduktTriphenylmethyl perchlorateHCID 10904004—
Edukt6,8-di-t-butyl-2,3-dihydro-4-oxo-4H-1-benzopyran-2-carboxylic acid, ethyl esterHCID 86733276—
Produkt6,8-di-t-butyl-4-oxo-4H-1-benzopyran-2-carboxylic acid, ethyl esterHCID 53843942—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 3.32 parts of 6,8-di-t-butyl-2,3-dihydro-4-oxo-4H-1-benzopyran-2-carboxylic acid, ethyl ester, 1.56 parts of triphenylmethyl perchlorate and 30 parts of acetic anhydride was heated at 100°C for thirty minutes. After cooling, the reaction mixture was poured into sodium bicarbonate solution and the resulting mixture was washed with water, dried and the ether was evaporated to give an oil which was chromatographed on silica gel using a 1:1 mixture of chloroform and light petroleum (b.p. 40°-60°C) for elution. This yielded 0.14 parts of 6,8-di-t-butyl-4-oxo-4H-1-benzopyran-2-carboxylic acid, ethyl ester, m.p. 130°-131.5°C (after crystallisation from light petroleum (b.p. 40°-60°C). This product was shown by spectral means to be the same as that prepared in Example 13.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03952104
Quelldatensatzuspto-grants-1976_04
ORD IDord-13a592c0f3024c1fa0dc41fa9ebe6241
Quellennotizuspto-grants-1976_04