HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326396Generated: October 29, 2026
Hydrochloric Acid → HCID 14693075, compound
https://huagongshe.com/reaction/326396
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-Hydroxy[1,1′-biphenyl]-3-carboxylic acid | HCID 11586549 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14693075 | HCID 14693075 | — |
Reaction Steps
A solution of 3-phenyl-4-hydroxybenzoic acid (131.1 g, 0.061 mole) and a 50 weight percent aqueous solution of NaOH (10.5 g, 0.131 mole) in 350 ml of deionized water was added to a 500 ml, three-necked, round-bottom flask equipped with a thermometer and a polytetrafluoroethylene-coated magnetic stir bar. The solution was stirred to homogeneity and then immersed in an ice water bath. With the solution temperature at 10° C., acetic anhydride (12.7 g, 0.124 mole) was added rapidly with stirring. Immediately, a white precipitate began to form. The reaction mixture was stirred for one hour at 10° C., then neutralized with concentrated HCl. The precipitate was filtered, washed in 500 ml of deionized water for one hour, filtered, and dried in an 80° C. vacuum oven for three hours yielding an off-white solid. The solid was recrystallized from a toluene and hexane mixture to give a fluffy white solid, 3-phenyl-4-acetoxybenzoic acid with a m.p. of 185° C. to 187° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05268443 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-d646333144384e0490ed2df99df02e64 |
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| Source note | uspto-grants-1993_12 |
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