HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443595Generated: October 29, 2026
Hydrochloric Acid → 2-(5-Benzyloxypentyl)-2-(3,3,3-trifluoropropyl)malononitrile
https://huagongshe.com/reaction/1443595
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzyl 5-Bromoamyl Ether | HCID 14221121 | — |
| Reactant | 2-(3,3,3-Trifluoropropyl)malononitrile | HCID 22185761 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-(5-Benzyloxypentyl)-2-(3,3,3-trifluoropropyl)malononitrile | HCID 58879044 | 81.5% |
Reaction Steps
3.5 g of 2-(3,3,3-trifluoropropyl)malononitrile, 5.5 g of 5-bromopentyl benzyl ether and 0.70 g of potassium iodide were dissolved in 20 ml of dimethyl sulfoxide, 3.3 g of potassium carbonate was added, and the mixture was stirred at room temperature for 9 hours. Thereafter, dilute hydrochloric acid was added to the reaction mixture, followed by extraction with methyl tert-butyl ether. The organic layer was washed successively with water, aqueous saturated sodium hydrogen carbonate and aqueous saturated sodium chloride, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 5.9 g of 2-(5-benzyloxypentyl)-2-(3,3,3-trifluoropropyl)malononitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07662402B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-191b6dfc0f254c298d0b3c0ebf7af502 |
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| Source note | uspto-grants-2010_02 |
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