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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018788Generated: October 26, 2026

Acetic Anhydride → N-(4-cyano-2-iodophenyl)acetamide

https://huagongshe.com/reaction/1018788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-Amino-3-iodobenzonitrileHCID 4416395—
CatalystSulfuric AcidHCID 1118—
SolventWaterHCID 962—
ProductN-(4-cyano-2-iodophenyl)acetamideHCID 2299194395%

Reaction Steps

A mixture of 8.54 g (0.035 mole) of 4-amino-3-iodobenzonitrile (31), 16 mL (16.32 g, 0.16 mole) of acetic anhydride and five drops of concentrated sulfuric acid was heated at 700 under reflux for 10 minutes (the mixture became thick when the temperature reached 400 and some manual stirring was required). The reaction mixture was poured over 400 mL of cold water and stirred for 5 minutes to give a white solid which was filtered and dried, yielding 9.48 g (95%) of 32 as white powder, mp 176-181°. Infrared (IR) and NMR analysis gave the following results: IR (potassium bromide): 3276 (NH), 2230 (CN), 1663 (C=O), 1517, 1297 cm−1. 1H nmr (90 MHz, CDCI3):δ 8.73 (1H, br s, NH), 8.13-8.05 (2H, m, H-5 and H-2), 7.65 (1 H; dd, 3JH5-H6=8.4 Hz, 4JH2-H6=1.8 Hz; H-6), 2.25 (3H, s, CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06482982B1
Source datasetuspto-grants-2002_11
ORD IDord-2b2caf05ec204e249163895b844ccc2a
Source noteuspto-grants-2002_11