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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619137Generated: November 1, 2026

Triethylamine → 3-Iodo-4-methylbenzonitrile

https://huagongshe.com/reaction/1619137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantPotassium CarbonateHCID 11430—
Reactant3-iodo-4-methylbenzamideHCID 833329—
SolventDichloromethaneHCID 6344—
Product3-Iodo-4-methylbenzonitrileHCID 1212962180.5%

Reaction Steps

2,2,2-trifluoroacetic anhydride (8.00 mL, 57.5 mmol) was added dropwise to a stirred solution of 3-iodo-4-methylbenzamide (preparation 48a, 6.00 g, 23.0 mmol) and triethylamine (8.10 mL, 57.5 mmol) in dichloromethane (50 mL) at 0° C. The mixture was warmed to room temperature and stirred for 2 hours. Further dichloromethane and saturated aqueous potassium carbonate solution were added and the organic layer was washed with 2M aqueous hydrochloric acid, 2M aqueous sodium hydroxide solution, brine, dried (MgSO4) and evaporated to give the title compound (4.50 g, 80%) as a pale orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772288B2
Source datasetuspto-grants-2014_07
ORD IDord-bc79983383474776b1875e5879140fdf
Source noteuspto-grants-2014_07