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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197482Generated: October 30, 2026

2-Aminothiophenol → HCID 19106821, compound

https://huagongshe.com/reaction/1197482

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiophenolHCID 8713—
ReactantSodium HydroxideHCID 14798—
Reactant(3-bromoprop-1-en-2-yl)benzeneHCID 234998—
SolventEthanolHCID 702—
ProductHCID 19106821HCID 1910682160.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

The compound, 2-aminothiophenol, (12.5 g) was added to a solution of sodium hydroxide (4.5 g) in ethanol (100 ml) keeping the temperature less than 30° C. Then 1-bromo-2phenyl-2-propene (21 g) was added and the mixture was stirred at 60° C. for 3 h. The precipitated solid was filtered and washed with ethanol. The solvent was removed and the residue was chromatographed on silica gel with hexanes/ethyl acetate (7:1) to yield the title compound (14.5 g). As an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05276039
Source datasetuspto-grants-1994_01
ORD IDord-560cbb259f4347eea88862b1489ab87f
Source noteuspto-grants-1994_01