HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384014Generated: October 30, 2026
(3-Chloropropyl)benzene → HCID 21188518, compound
https://huagongshe.com/reaction/1384014
Participants
| Role | Name | HCID | Charge |
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| Reactant | (3-Chloropropyl)benzene | HCID 7706 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 21188464 | HCID 21188464 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21188518 | HCID 21188518 | — |
Reaction Steps
In a 50 ml round bottom flask, under a nitrogen atmosphere, were added 4-(prop-2-enyl)-2-[(4-chlorophenoxy)methyl]-1-[3-(piperidin-4-yl)propyl]benzimidazole (898 mg, 2.12 mmol), potassium carbonate (1.46 g, 10.58 mmol), 3-(phenyl)propyl chloride (0.2 ml, 506 mg, 2.54 mmol) and N,N-dimethylformamide (7 ml). The resulting mixture was heated to 60° C. and maintained at this temperature overnight. The progress of the reaction was monitored by thin layer chromatography. An additional 1 equivalent of potassium carbonate and 0.2 ml of 3-(phenyl)propyl chloride were added and the resulting contents were stirred at 60° C. for an additional two hours. The reaction was quenched by the addition of water. The aqueous fraction was extracted wtih ethyl acetate. The organic fractions were combined, washed with water, and then dried over sodium sulfate. The solvents were removed in vacuo. The desired title product was further purified by radial chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06255494B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-90a6d6c7c48141a0a386f0d476a7715c |
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| Source note | uspto-grants-2001_07 |
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