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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494701Generated: October 25, 2026

Acetic Acid → 1-[2-(3-Butenylthio)-2-methylpropylamino]-2-(2-mercapto-2-methylpropylamino)benzene

https://huagongshe.com/reaction/1494701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-Amino-1-(2-mercapto-2-methylpropylamino)benzeneHCID 10012927—
Reactant2-(3-Butenylthio)-2-methylpropanalHCID 10464580—
SolventMethanolHCID 887—
Product1-[2-(3-Butenylthio)-2-methylpropylamino]-2-(2-mercapto-2-methylpropylamino)benzeneHCID 1004942384%

Reaction Steps

2-Amino-1-(2-mercapto-2-methylpropylamino)benzene (3.5 g, 1.78×10-2 mol, 100 M %) and 2-(3-butenylthio)-2methylpropanal (4.23 g, 2.67×10-2 mol, 150 M %) were dissolved in 200 ml methanol. Glacial acetic acid (2.05 ml, 3.56×10-2 mol, 200 M %) and sodium cyanoborohydride (3.36 g, 5.35×10-2 mol, 300 M %) were then added. After 17 hours, the reaction was quenched by the addition of 100 ml 0.5N HCl. The acidic solution was then extracted with 2×100 ml diethyl ether. The combined organic extracts were washed with 100 ml saturated NaHCO3, followed by 100 ml saturated NaCl. The ether layer was then dried over anhydrous Na2SO4. The solvent was removed on the rotary evaporator, and the residue was purified by filtration through a 600 ml sintered-glass funnel silica bed, using 90% hexane/diethyl ether as the eluting solvent, to give 5 g (84% yield) 1-[2-(3-butenylthio)-2-methylpropylamino]-2-(2-mercapto-2-methylpropylamino)benzene as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026913
Source datasetuspto-grants-1991_06
ORD IDord-3b94da8b57f24345b640cb52c90db525
Source noteuspto-grants-1991_06