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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616985Generated: October 30, 2026

Hydrochloric Acid → 1-(4-Hydroxyphenyl)-4-phenyl-1,2,4-triazolidine-3,5-dione

https://huagongshe.com/reaction/1616985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhenolHCID 996—
Reactant4-Phenyl-1,2,4-triazoline-3,5-dioneHCID 77913—
SolventAcetonitrileHCID 6342—
Product1-(4-Hydroxyphenyl)-4-phenyl-1,2,4-triazolidine-3,5-dioneHCID 6725816915%

Reaction Steps

To a solution of phenol (11.3 mg, 0.120 mmol) in 100 mM pH 7.0 NaH2PO4/Na2HPO4 buffer (3.0 mL)-CH3CN (3.0 mL) was slowly dropped the 0.3 M solution of PTAD 17a (0.442 mL, 0.132 mmol) in CH3CN at room temperature. The resulting solution was stirred at room temperature for 30 minutes. The reaction mixture was acidified with 1M HCl and extracted with ethyl acetate twice. The organic layer was dried over Na2SO4 and concentrated in vacuo. The obtained crude material was purified by flash column chromatography (ethyl acetate) to give para-adduct 27 (4.8 mg, 15%) and para-ortho-di-adduct 27′ (10.1 mg, 19%) as a white solid. 1H NMR (300 MHz, DMSO-d6): δ 11.35 (br, 1H), 9.60 (s, 1H), 7.53-7.35 (m, 7H), 6.83 (m, 2H), 13C NMR (75 MHz, DMSO-d6): δ 156.11, 152.73, 150.41, 132.22, 129.22, 128.78, 128.66, 127.19, 122.99, 116.22. HRMS: calcd for C14H11N3O3 (MH+) 270.0873. found 270.0873.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765920B2
Source datasetuspto-grants-2014_07
ORD IDord-bfb3a288e50d49f6a258a63a18fbf492
Source noteuspto-grants-2014_07