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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(p-Methoxyphenyl)-5-phenyl-1-hydroxy-1,2-dihydroimidazole-2-thione | HCID 14938561 | — |
| Reactant | HCID 178514129 | HCID 178514129 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Phenyl-1-hydroxy-1,2-dihydroimidazole-2-thione | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05283271 |
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| Source dataset | uspto-grants-1994_02 |
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| ORD ID | ord-bb4e99782d974f15be6b3c40c85d01c4 |
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| Source note | uspto-grants-1994_02 |
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