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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750967Generated: October 26, 2026

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

https://huagongshe.com/reaction/750967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylbarbituric acidHCID 69860—
Reactant1-[2-(4-Allyloxy-phenylmethanesulfinyl)-ethyl]-1H-[1,2,3]triazoleHCID 22242085—
CatalystHCID 178418397HCID 178418397—
SolventDichloromethaneHCID 6344—
Product4-(2-[1,2,3]Triazol-1-yl-ethanesulfinylmethyl)-phenolHCID 2224207597.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

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 the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405231B2
Source datasetuspto-grants-2008_07
ORD IDord-23fd9aba4cfe413892262e8ff7a3b9b2
Source noteuspto-grants-2008_07