HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894913Generated: October 28, 2026
Hydrochloric Acid → 2-(3-Methoxyphenyl)-5-phenylpentane
https://huagongshe.com/reaction/894913
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | (1-Bromopropyl)benzene | HCID 562384 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 2-(3-Methoxyphenyl)-5-phenylpentane | HCID 20496826 | — |
Reaction Steps
A solution of 1-bromopropylbenzene (51.7 g.) in ether (234 ml.) is added dropwise over a 2-hour period to a refluxing mixture of magnesium (7.32 g.) in ether (78 ml.). The reaction mixture is refluxed for 30 minutes longer and then a solution of 3-methoxy-acetophenone (41.6 g.) in ether (78 ml.) is added dropwise and the mixture heated to reflux for 1.5 hours. The reaction is quenched by addition of saturated ammonium chloride (234 ml.), the ether layer is separated and the aqueous phase extracted with ether (3×200 ml.). The combined ether extracts are dried over magnesium sulfate and concentrated under vacuum to yield an oil. The oil is hydrogenated in a mixture containing ethanol (300 ml.), concentrated hydrochloric acid (2 ml.) and 5% palladium-on-carbon (5 g.). The catalyst is filtered off and the ethanol removed under vacuum. The residue is distilled under vacuum to give the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04284829 |
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| Source dataset | uspto-grants-1981_08 |
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| ORD ID | ord-162c0897190f4eea9057c0b82f4fdd8f |
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| Source note | uspto-grants-1981_08 |
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