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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460890Generated: October 26, 2026

Hydrochloric Acid → 4-Acetyl-4'-hydroxy-2-nitro biphenyl

https://huagongshe.com/reaction/1460890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAluminum bromideHCID 24409—
Reactant1-(4'-Methoxy-2-nitro-[1,1'-biphenyl]-4-yl)ethanoneHCID 18956616—
ReactantEthyl acetate hexaneHCID 21226206—
SolventBenzeneHCID 241—
Product4-Acetyl-4'-hydroxy-2-nitro biphenylHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05071988
Source datasetuspto-grants-1991_12
ORD IDord-90d0ecb6658e475bb63acbcb220435d1
Source noteuspto-grants-1991_12