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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419561Generated: November 1, 2026

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

https://huagongshe.com/reaction/2419561

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 three 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 numberUS04107175
Source datasetuspto-grants-1978_08
ORD IDord-4956deb3626c4de9a9c3ca65680a5657
Source noteuspto-grants-1978_08