HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610849Generated: October 29, 2026
Diethyl Ether → 4-(p-Chlorophenyl)-4-methyl-2-pentenal
https://huagongshe.com/reaction/610849
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | 4-(p-Chlorophenyl)-3-fluoro-4-methyl-2-pentenenitrile | HCID 54269028 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-(p-Chlorophenyl)-4-methyl-2-pentenal | HCID 53939919 | 97% |
Reaction Steps
A solution of 4-(p-chlorophenyl)-3-fluoro-4-methyl-2-pentenenitrile, (Z)- (15.6 g, 69.7 mmol) in diethyl ether is treated dropwise with diisobutylaluminum hydride (83.6 mmol, 83.6 mL of a 1M solution in hexane) over 90 minutes at -45° C. under nitrogen, stirred at -40° C. for 35 minutes, and diluted sequentially with water and 2N hydrochloric acid at -10° C. The resultant aqueous mixture is stirred at room temperature for one hour and extracted with diethyl ether. The organic extracts are combined, washed sequentially with water, 2N hydrochloric acid and water, dried over anhydrous sodium sulfate, and concentrated in vacuo to give the title product as a brown oil (15.34 g, 97% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05998673 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-f6e435d6224c4651ad1c500264928ec7 |
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| Source note | uspto-grants-1999_12 |
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