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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | N-(2-Aminoethyl)piperidine | HCID 33944 | — |
| Reactant | 5-Chloro-N-methyl-N-phenyl-1,3-benzodithiol-2-iminium iodide | HCID 20313844 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(5-Chloro-1,3-benzodithiol-2-ylidene)-1-piperidineethanamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04104467 |
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| Source dataset | uspto-grants-1978_08 |
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| ORD ID | ord-b92fece7341c48f0936c4fd1e0ee8a04 |
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| Source note | uspto-grants-1978_08 |
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