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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909742Generated: November 1, 2026

Anisole → (4-Iodophenyl)(4-methoxyphenyl)methanone

https://huagongshe.com/reaction/1909742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisoleHCID 7519—
Reactant4-Iodobenzoyl chlorideHCID 74373—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventNitrobenzeneHCID 7416—
Product(4-Iodophenyl)(4-methoxyphenyl)methanoneHCID 2213267497.9%

Reaction Steps

To a solution of 4-iodo-benzoyl chloride (5 g, 15 mmol) and AlCl3 (2.6 g, 20 mmol) in nitrobenzene (20 mL) was added a solution of methoxy-benzene (1.5 g, 14.5 mmol) in nitrobenzene (5 mL) slowly at 0° C. The resulting mixture was allowed to warm to rt and stir at rt for 16 h. The mixture was poured onto 150 mL ice-water solution and extracted with CH2Cl2 (5×100 mL). The combined organic layers were washed with water (2×100 mL) and brine (50 mL) and dried over anhy. Na2SO4. The solvent was removed in vacuo to provide the crude product, which was purified by recrystallization from cyclohexane to yield the title product (4.8 g, 88%); MS; APCI+ (Calcd: 338.15; Found m/z: 339.35, M+1); 1HNMR (400 MHz, CDCl3); δ 3.89 (s, 3H), 6.96 (d, J=8.8, 2H), 7.47 (d, J=8.4, 2H), 7.79 (d, J=9.2, 2H), 7.83 (d, J=8.4, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598359B2
Source datasetuspto-grants-2013_12
ORD IDord-313e13ab00f94972b274128478bf2d96
Source noteuspto-grants-2013_12