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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722743Generated: October 27, 2026

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

https://huagongshe.com/reaction/1722743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantLithium diisopropylamideHCID 2724682—
Reactant2-(3,4,5-Trimethoxyphenylthio)ethyl chlorideHCID 14994183—
Reactant1-(2-Thienyl)propyl isocyanideHCID 15288588—
ReactantHCID 178418244HCID 178418244—
SolventAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1-Ethyl-3-(3,4,5-trimethoxyphenylthio)-1-(2-thienyl)propyl isocyanideHCID 1069101074.4%

Reaction Steps

A solution of diisopropylamine (2.65 g) in tetrahydrofuran is cooled to -60° C. and 1.6M n-butyl lithium/hexane solution (14 ml) is added dropwise thereto in nitrogen atmosphere. The mixture is stirred at the same temperature, whereby the solution containing lithium diisopropylamide is obtained. A solution of 1-(2-thienyl)propyl isocyanide (2.8 g) in tetrahydrofuran is added dropwise to the solution obtained above at -60° C. and the mixture is stirred at the same temperature for 20 minutes. A solution of 2-(3,4,5-trimethoxyphenylthio)ethyl chloride (5.9 g) in tetrahydrofuran is added dropwise to the mixture at -60° C. and the mixture is stirred at -30° C. in nitrogen atmosphere for 2 hours. Acetic acid is added to the mixture to cease the reaction and ether is added to the reaction mixture. The mixture is washed, dried and concentrated under reduced pressure to remove solvent. The residue is purified by silica gel chromatography, whereby 1-ethyl-3-(3,4,5-trimethoxyphenylthio)-1-(2-thienyl)propyl isocyanide (5.2 g) is obtained as red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04857543
Source datasetuspto-grants-1989_08
ORD IDord-4bc0e71f055b4fac883f1a2cebd824c3
Source noteuspto-grants-1989_08