HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635249Generated: October 25, 2026
Phenethyl bromide → 1,5-Diphenylpentan-3-ol
https://huagongshe.com/reaction/635249
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Benzenepropanal | HCID 7707 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1,5-Diphenylpentan-3-ol | HCID 12838510 | — |
Reaction Steps
A solution of 2-(bromoethyl)benzene (1.73 g; 9.33 mmol) in diethylether (10 mL) was added to a stirred slurry of magnesium turnings (250 mg; 10.18 mmol) in 5 mL of ether. The reaction was initiated with a heat gun, and after the addition was complete the mixture was heated on an oil bath for 30 minutes. 3-Phenyl-1-propanal (1.25 g; 9.33 mmol) was added in 10 mL of ether, and reflux was continued for 1 hour. The reaction was cooled and quenched with saturated ammonium chloride, extracted into 2x ethyl acetate, and the combined organic portions were dried and concentrated. Chromatographic purification on a silica gel column (10% ethyl acetate in hexane) delivered 1.42 g (63%) of the diphenyl alcohol. 1H NMR (300 MHz, CDCl3): δ1.84 (m, 4H); 2.61-2.76 (m,4H); 3.65 (m, 1H); 7.19-7.29 (m, 10H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06187796B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-9897418fa5c541b1b709f2a38f9a17d4 |
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| Source note | uspto-grants-2001_02 |
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