HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635905Generated: October 31, 2026
Hydrochloric Acid → 3-Acetyl-4-hydroxybenzoic acid
https://huagongshe.com/reaction/635905
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Benzoic acid, 4-(acetyloxy)- | HCID 16865 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,2,4-Trichlorobenzene | HCID 13 | — |
| Product | 3-Acetyl-4-hydroxybenzoic acid | HCID 9179245 | — |
Reaction Steps
36.6 g (0.274 mol) of AlCl3 are suspended in 50 ml of 1,2,4-trichloro-benzene and treated with 9 g (50 mmol) of 4-acetoxybenzoic acid. After dropwise addition of 7.84 g (0.1 mol) of acetyl chloride, the reaction mixture is heated to 130-140° C., the evolution of HCl gas occurring from approximately 60° C. The mixture is stirred for approximately 1 hour at 130° C. and then allowed to cool to 60-70° C., and the mixture is poured cautiously into stirred ice water. It is extracted several times with ethyl acetate, then the combined organic phases are extracted with saturated aqueous sodium bicarbonate solution and the combined aqueous phases are adjusted carefully to pH<1 using concentrated HCl, the 3-acetyl-4-hydroxybenzoic acid separating as sparingly soluble material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06191164B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-32b4594bab174a5b8714095c22992b82 |
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| Source note | uspto-grants-2001_02 |
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