HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732245Generated: October 30, 2026
Acetonitrile → 4-((5-Chloropentyl)oxy)benzonitrile
https://huagongshe.com/reaction/732245
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Cyanophenol | HCID 13019 | — |
| Reactant | 1-Bromo-5-chloropentane | HCID 96070 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-((5-Chloropentyl)oxy)benzonitrile | HCID 19381510 | 90% |
Reaction Steps
While 70 g of 4-hydroxybenzonitrile (7) were added to 500 ml of acetonitrile and stirred, 85.3 g of potassium carbonate and 77.4 ml of 1-bromo-5-chloropentane were added. Subsequently, the temperature was gradually increased and stirring under reflux was continued for 8 hr, and then stirring was further continued at room temperature for 18 hr. After the reaction was completed, the resultant reaction mixture was added with 500 ml of ethylacetate and then washed with water. Thereafter, the ethylacetate layer was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The concentrated compound was dissolved in 280 ml of methanol, stirred at 0° C. for 2 hr, and then filtered, thus obtaining 118 g (yield: 90%) of a title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07585979B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-225054464824456abd76b61186e45866 |
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| Source note | uspto-grants-2009_09 |
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