Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1974575Generated: October 26, 2026

3-(p-Methoxyphenyl)-5-phenyl-1-hydroxy-1,2-dihydroimidazole-2-thione → Phenyl-1-hydroxy-1,2-dihydroimidazole-2-thione

https://huagongshe.com/reaction/1974575

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(p-Methoxyphenyl)-5-phenyl-1-hydroxy-1,2-dihydroimidazole-2-thioneHCID 14938561—
ReactantHCID 178514129HCID 178514129—
SolventDichloromethaneHCID 6344—
ProductPhenyl-1-hydroxy-1,2-dihydroimidazole-2-thioneHCID 24783967—

Reaction Steps

The thiohydroxamine acid, 3-(p-methoxyphenyl)-5-phenyl-1-hydroxy-1,2-dihydroimidazole-2-thione, was prepared from the thiocarbamate in a manner similar to that used in Example I. The 3-(p-methoxyphenyl)-5-phenyl-1-hydroxy-1,2-dihydroimidazole-2-thione was recrystallized from methylene chloride/hexane to give white crystalline material. mp: 168° C. (dec); IR (CH2Cl2): 2800-1756-1510-1383-1361-1241-1133 cm-1 ; 1H NMR (200 MHz, CDCl3 : DMSO 1:1): 3.82 (3H, OCH3, s); 6.5 (2H, d); 7.15 (1H, CH=, s); 7.4 (3H, m); 7.54 (2H, d); 7.71 (2H, d); 11.85 (1H, OH, br); 13C NMR (CDCl3 : DMSO 1:1): 54 (OCH3): 110.6 (CH=); 112.6 (CH); 125.6 (CH); 125.7 (CH); 127 (CH); 127.2 (CH); 129.5 (Cq); 157.6 (CH); Anal. Calcd for C16H14N2O2 5: C, 64.40; H, 4.73; N, 9.39; S,10.74 Found C, 64.48; H, 4.24; N,9.43; S, 10.68.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05283271
Source datasetuspto-grants-1994_02
ORD IDord-bb4e99782d974f15be6b3c40c85d01c4
Source noteuspto-grants-1994_02