HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406350Generated: October 30, 2026
Heptane → 2-(4-Bromo-2-trifluoromethylphenyl)-5-chloropentanenitrile
https://huagongshe.com/reaction/406350
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Heptane | HCID 8900 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Chloro-3-iodopropane | HCID 81363 | — |
| Reactant | 2-[4-Bromo-2-(trifluoromethyl)phenyl]acetonitrile | HCID 58488407 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Bromo-2-trifluoromethylphenyl)-5-chloropentanenitrile | HCID 66618750 | — |
Reaction Steps
A solution of (4-bromo-2-trifluoromethylphenyl)acetonitrile (2.28 g) in tetrahydrofuran (6 mL) was added to a suspension of sodium hydride (containing 60% in mineral oil, 362 mg) in tetrahydrofuran (12 mL) under ice-cooling. The mixture was stirred at the same temperature for 20 minutes. 1-Chloro-3-iodopropane (0.94 mL) was added dropwise to the reaction solution, and then the reaction solution was stirred at room temperature for 40 minutes. Ice water and heptane were added to the reaction solution, and the organic layer was separated. The resulting organic layer was washed with brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (carrier: Wakogel™ C-200; elution solvent:heptane:ethyl acetate=49:1→19:1) to obtain 2.67 g of the title compound. The property values of the compound are as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754100B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-453ed83376d14b0b94503e9d9e995ca8 |
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| Source note | uspto-grants-2014_06 |
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