HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584282Generated: October 30, 2026
Hydrochloric Acid → 1-(4-Hydroxy-3-propyl-phenyl)-propan-1-one
https://huagongshe.com/reaction/584282
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Propylphenol | HCID 12570 | — |
| Reactant | Propionyl chloride | HCID 62324 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Product | 1-(4-Hydroxy-3-propyl-phenyl)-propan-1-one | HCID 22345621 | 35% |
Reaction Steps
7.1 g (53 mmol) of aluminum chloride are placed in 70 ml of nitrobenzene in a round-bottomed flask and under a stream of nitrogen. The mixture is heated at 70° C. until dilution is complete. It is then cooled to 0° C. and 7.2 ml (52 mmol) of 2-propylphenol are added. The mixture is allowed to warm to room temperature and is then heated to 40° C. 4.6 ml (52 mmol) of propionyl chloride are then added dropwise. The reaction medium is heated at 40° C. for 2 hours and then stirred for 48 hours at room temperature. It is then poured into ice with 20 ml of concentrated hydrochloric acid. After extraction with ethyl ether, the organic phase is washed with 2N sodium hydroxide. The aqueous phases are acidified with hydrochloric acid and extracted with ether. The organic phase is dried over magnesium sulfate, filtered and then evaporated. The black solid obtained is triturated in heptane, filtered off and dried. 3.5 g (35%) of the expected product are obtained in the form of a black powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06924400B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-df6452d21af04a61b5a2296380ada0a7 |
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| Source note | uspto-grants-2005_08 |
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