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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722735Generated: October 27, 2026

1-Ethyl-3-(3,4,5-trimethoxyphenylthio)-1-(2-thienyl)propyl isocyanide → 1-Ethyl-3-(3,4,5-trimethoxyphenylthio)-1-(2-thienyl)propylamine

https://huagongshe.com/reaction/1722735

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3,4,5-trimethoxyphenylthio)-1-(2-thienyl)propyl isocyanideHCID 10691010—
ReactantHydrochloride methanolHCID 21893726—
Product1-Ethyl-3-(3,4,5-trimethoxyphenylthio)-1-(2-thienyl)propylamineHCID 1465007384.9%

Reaction Steps

15% Hydrogen chloride/methanol solution (12 ml) is added to 1-ethyl-3-(3,4,5-trimethoxyphenylthio)-1-(2-thienyl)propyl isocyanide (2.3 g) under ice-cooling and the mixture is stirred at room temperature for 3 hours. The mixture is concentrated under reduced pressure to remove solvent and the residue is adjusted to pH 10 with an aqueous potassium carbonate solution. The aqueous mixture is extracted with ethyl acetate and the extract is washed with an aqueous saturated sodium chloride solution, dried and then concentrated to remove solvent. The residue is purified by silica gel column chromatography (solvent, n-hexane:ethyl acetate=4:1), whereby 1-ethyl-3-(3,4,5-trimethoxyphenylthio)-1-(2-thienyl)propylamine (1.9 g) is obtained as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04857543
Source datasetuspto-grants-1989_08
ORD IDord-6f1c2163646344edb4d3708998758bc3
Source noteuspto-grants-1989_08