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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 33494Erstellt: 24. Oktober 2026

Dimethylbarbituric acid → 4-(2-[1,2,3]Triazol-1-yl-ethanesulfinylmethyl)-phenol

https://huagongshe.com/de/reaction/33494

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylbarbituric acidHCID 69860—
Edukt1-[2-(4-Allyloxy-phenylmethanesulfinyl)-ethyl]-1H-[1,2,3]triazoleHCID 22242085—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(2-[1,2,3]Triazol-1-yl-ethanesulfinylmethyl)-phenolHCID 2224207597,5%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A solution of 1.00 g (3.43 mmol) 1-[2-(4-allyloxy-phenylmethanesulfinyl)-ethyl]-1H-[1,2,3]triazole in 60 ml dichloromethane was added to a solution of 1.61 g (10.3 mmol) 1,3-dimethylbarbituric acid and 102 mg (0.09 mmol) Pd(PPh3)4 in 30 ml dichloromethane and stirred for 5 h at 50° C. The mixture was extracted with 3×50 ml sat. NaHCO3-solution and 20 ml water. The organic phase was discarded and the aqueous phase acidified with 2M HCl to pH=4, concentrated to a volume of 50 ml and adjusted to pH=1. After five extractions with ethyl acetate, the organic extracts were combined and dried over MgSO4. After evaporation the residue was purified by chromatography on silica gel (dichloromethane/methanol 100:2) to yield 0.84 g (97%) of 4-(2-[1,2,3]Triazol-1-yl-ethanesulfinylmethyl)-phenol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07429605B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-d9c2db7229934015a6ccd109b303a010
Quellennotizuspto-grants-2008_09