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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419136Generated: October 30, 2026

Water → N-(5-Chloro-1,3-benzodithiol-2-ylidene)-1-piperidineethanamine

https://huagongshe.com/reaction/2419136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantN-(2-Aminoethyl)piperidineHCID 33944—
Reactant5-Chloro-N-methyl-N-phenyl-1,3-benzodithiol-2-iminium iodideHCID 20313844—
SolventDimethylformamideHCID 6228—
ProductN-(5-Chloro-1,3-benzodithiol-2-ylidene)-1-piperidineethanamineHCID 20313855—

Reaction Steps

A solution of 5-chloro-N-methyl-N-phenyl-1,3-benzodithiol-2-iminium iodide (8.39g), N-(2-aminoethyl)piperidine (2.56g) and anhydrous sodium carbonate (1.06g) in 200 ml of anhydrous dimethylformamide is heated at 120° C under a nitrogen atmosphere for 3 hours. The reaction mixture is poured into 1000 ml of water and extracted with three 300 ml portions of dichloromethane. The combined organic extracts are washed with two 500 ml portions of water, dried over anhydrous sodium sulfate, and concentrated in vacuo to yield an oil. This oil is chromatographed on silica gel (1000 ml) eluting with (1) pentane (1000 ml), (2) chloroform (1000 ml), and finally methanol/chloroform (1:4, 2000 ml). The solid product from elution (3) is recrystallized from pentane to yield 4g of the title compound, melting point 42°-44° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04104467
Source datasetuspto-grants-1978_08
ORD IDord-b92fece7341c48f0936c4fd1e0ee8a04
Source noteuspto-grants-1978_08