Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306428Generated: October 31, 2026

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

https://huagongshe.com/reaction/2306428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2-Chloro-4-iodoanilineHCID 282930—
SolventTetrahydrofuranHCID 8028—
ProductN-(2-Chloro-4-iodophenyl)acetamideHCID 1843436884%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-chloro-4-iodoaniline (25 g, 96.66 mmol) in tetrahydrofuran (100 mL) was cooled to 0° C. and then treated with acetic anhydride (50.6 g, 500 mmol). The reaction mixture was stirred at 0° C. for I0 min and then allowed to warm to 25° C. where it was stirred for 15 h. The reaction mixture was then concentrated in vacuo to remove tetrahydrofuran. The residue was crystallized from ether (50 mL) and hexanes (50 mL). The solids were collected and washed with hexanes to afford N-(2-chloro-4-iodo-phenyl)-acetamide (23.87 g, 84%) as a white crystalline solid: EI-HRMS m/e calcd for C8H7ClINO (M+) 295.1526, found 295.1532.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441180B1
Source datasetuspto-grants-2002_08
ORD IDord-c4357a289d09444bb41758813d95b055
Source noteuspto-grants-2002_08