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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885926Generated: November 2, 2026

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

https://huagongshe.com/reaction/885926

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 5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242116B2
Source datasetuspto-grants-2012_08
ORD IDord-7479d65ae27a4ec8b019a22d89d086b0
Source noteuspto-grants-2012_08