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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
ReactantS-2-amino-4-benzylphenyl dimethylcarbamothioateHCID 58415349—
SolventEthylene GlycolHCID 174—
Product2-(2-(2-Amino-4-benzylphenyl)disulfanyl)-5-benzylbenzenamineHCID 58415295—

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919519B2
Source datasetuspto-grants-2011_04
ORD IDord-85536e841b4a4a689bf79a9da63eb445
Source noteuspto-grants-2011_04