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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919595Generated: October 31, 2026

p-Aminoacetophenone → Ethanone, 1-(4-amino-3-iodophenyl)-

https://huagongshe.com/reaction/1919595

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-AminoacetophenoneHCID 7468—
ReactantCalcium CarbonateHCID 10112—
ReactantIodine chlorideHCID 24640—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductEthanone, 1-(4-amino-3-iodophenyl)-HCID 1103265244.4%

Reaction Steps

To a stirred suspension of CaCO3 (4.5 g, 45.27 mmol) in H2O (15 mL) was added a solution of 4-acetylaniline (4.1 g, 30.18 mmol) in MeOH (25 mL), followed by a solution of iodine monochloride (5.2 g, 31.88 mmol) in MeOH (20 mL) dropwise. The reaction was stirred at r.t. for 45 minutes, then diluted with Et2O (150 mL). The organic fraction was separated, washed with water (100 mL), then brine (100 mL), dried (Na2SO4), filtered and concentrated in vacuo to give the title compound (3.5 g, 44%) as a brown oil that was used without further purification. δH (DMSO-d6) 8.14 (1H, d, J 1.8 Hz), 7.70 (1H, dd, J 8.3 and 1.8 Hz), 6.75 (1H, d, J 8.3 Hz), 6.10 (2H, s), 2.41 (3H, s). LCMS (ES+) 261 (M)+, 283 (M+Na)+, RT 3.026 minutes (Method 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168634B2
Source datasetuspto-grants-2012_05
ORD IDord-eea59f3c349b4ae396481a41ffc5b60e
Source noteuspto-grants-2012_05