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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 274039Erstellt: 24. Oktober 2026

4-Hydroxybenzyl Alcohol → 4-(3-tert-Butyl-4-methoxybenzoyloxymethyl)phenol

https://huagongshe.com/de/reaction/274039

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Hydroxybenzyl AlcoholHCID 125—
EduktWaterHCID 962—
EduktPyridineHCID 1049—
Edukt3-Tert-butyl-4-methoxybenzoyl chlorideHCID 13633555—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(3-tert-Butyl-4-methoxybenzoyloxymethyl)phenolHCID 21474530—

Reaktionsschritte

1.24 g (0.01 mol) of 4-hydroxybenzenemethanol, 1 ml (0.01 mol) of pyridine and 50 ml of THF are introduced into a round-bottomed flask. While cooling in an icebath, a solution of 2.2 g (0.01 mol) of 3-tert-butyl-4-methoxybenzoyl chloride in 50 ml of THF is introduced dropwise and the mixture is stirred at room temperature for 24 h. The reaction medium is poured into water, the mixture is extracted with ethyl ether and the organic phase is separated after settling has taken place, dried over magnesium sulphate and evaporated. The residue obtained is purified by chromatography on a silica column and eluted with a mixture of dichloromethane and ethyl ether (97:3).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05387594
Quelldatensatzuspto-grants-1995_02
ORD IDord-6f43e7ba229e4366a2732b9a84ac901f
Quellennotizuspto-grants-1995_02