HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293675Generated: October 31, 2026
4-Ethylbenzaldehyde → 4-Ethyl-α-propylbenzenemethanol
https://huagongshe.com/reaction/2293675
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Ethylbenzaldehyde | HCID 20861 | — |
| Reactant | HCID 178455851 | HCID 178455851 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Ethyl-α-propylbenzenemethanol | HCID 22486907 | — |
Reaction Steps
To a flame-dried flask under an argon atmosphere is added 0.69 mL of commercially available 4-ethylbenzaldehyde and charged with 15 mL of diethyl ether. The solution is cooled to 0° C. and is treated with 3.0 mL (2.0M in diethyl ether) of propylmagnesium bromide. The reaction mixture is left to warm to room temperature overnight and then quenched by the addition of aqueous ammonium chloride. After dilution with diethyl ether the phases are separated; the organic layer is washed with saturated ammonium chloride, dried (magnesium sulfate) and finally concentrated under reduced pressure. The residue is flash column chromatographed using 25% to 30% diethyl ether in hexane to yield 1.08 g of the title product as a clear, colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05686486 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-010768999b264906882c5e797d45e26d |
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| Source note | uspto-grants-1997_11 |
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