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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 47611Erstellt: 24. Oktober 2026

Benzoyl chloride → HCID 178490912, Verbindung

https://huagongshe.com/de/reaction/47611

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl chlorideHCID 7412—
EduktCalcium HydroxideHCID 6093208—
EduktEthyl acetate hexaneHCID 21226206—
EduktHCID 178490910HCID 178490910—
KatalysatorWaterHCID 962—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktHCID 178490912HCID 178490912—

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

A solution containing 1.0 g of 2-(4-methoxybenzyl)-5-methyl-2H-pyrazol-3-ol in 30 ml of dioxan was treated with 679 mg of calcium hydroxide and 800 μl of benzoyl chloride, then heated at 110° C. for 2 h. To the mixture was added 20 drops of water and the mixture heated for a further 2 h. The solvent was evaporated under reduced pressure and the residue partitioned between dichloromethane/10% citric acid. The organic phase was washed with brine, then dried over anhydrous magnesium sulphate, filtered and evaporated to give yellow oil. The oil was purified twice by flash chromatography on silica gel, initially using methanol/dichloromethane (1:49) to give a red solid, then ethyl acetate/hexane (1:1 to 2:1) for the elutions to give 400 mg of [5-hydroxy-1-(4-methoxybenzyl)-3-methyl-1H-pyrazol-4-yl]-phenyl-methanone as a yellow gum. Mass spectrum (ES) m/z 323 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06699887B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-b57b2889c45d4f6bab0134cfbdabfb8e
Quellennotizuspto-grants-2004_03