HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075254Generated: November 3, 2026
Water → 2-(2-(2-Amino-4-benzylphenyl)disulfanyl)-5-benzylbenzenamine
https://huagongshe.com/reaction/2075254
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | S-2-amino-4-benzylphenyl dimethylcarbamothioate | HCID 58415349 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | 2-(2-(2-Amino-4-benzylphenyl)disulfanyl)-5-benzylbenzenamine | HCID 58415295 | — |
Reaction Steps
To a slurry of S-2-amino-4-benzylphenyl dimethylcarbamothioate (1.43 g, 4.99 mmol) in 15 mL ethylene glycol was added potassium hydroxide (0.840 g, 15.0 mmol) (solid, finely crushed). The reaction was heated to 60° C. under nitrogen. 10 mL 2-BuOH was added as cosolvent and the resulting solution was heated for 2 h. The reaction was fitted with a water-cooled reflux condensor and heated to 90° C. for 3 h. The reaction was cooled, and concentrated in vacuo. The material was partitioned between Et2O and water. The organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo to give an oil, which was purified by silica gel chromatography, ISCO, 0-30% EtOAc/hexanes to give 2-(2-(2-amino-4-benzylphenyl)disulfanyl)-5-benzylbenzenamine as a brown oil. MS (ESI) m/z: Calculated: 428.1; Observed: 429.0 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07919519B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-85536e841b4a4a689bf79a9da63eb445 |
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| Source note | uspto-grants-2011_04 |
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