HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587569Generated: October 26, 2026
Hydrochloric Acid → 4-Acetyl-4'-hydroxy-2-nitro biphenyl
https://huagongshe.com/reaction/1587569
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Aluminum bromide | HCID 24409 | — |
| Reactant | 1-(4'-Methoxy-2-nitro-[1,1'-biphenyl]-4-yl)ethanone | HCID 18956616 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-Acetyl-4'-hydroxy-2-nitro biphenyl | HCID 18956614 | — |
Reaction Steps
To a stirred solution of AlBr3 (12.6 g, 47.4 mmole) in benzene (45 mL) is added dropwise under nitrogen a solution of the methylether (5 g, 18.45 mmole) of Step A in benzene (12 mL) over 30 minutes. The resulting solution is stirred at room temperature for 3.5 hours. (TLC, 8:2 hexane-ethyl acetate). The mixture is cooled in an ice bath and the complex is decomposed by the dropwise addition of 6N-HCl (ca. 37 mL). The organic layer is separated and the aqueous phase is reextracted with ether (3×). The combined extracts are concentrated to a small volume and extracted again with 2.5N-NaOH (2×50 mL +1×10 mL). The basic extracts are cooled and acidified with concentrated HCl (to pH 2). The solid is collected and dried (4.27 g, 90%). It is used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05218124 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-6e0273b1132a4f158bd7572788800fd8 |
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| Source note | uspto-grants-1993_06 |
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