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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865062Generated: October 30, 2026

Acetonitrile → 2-(4-Iodophenyl)benzenecarbonitrile

https://huagongshe.com/reaction/1865062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant2-(4-Iodophenyl)benzamideHCID 57974859—
SolventWaterHCID 962—
Product2-(4-Iodophenyl)benzenecarbonitrileHCID 139335995.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

Add 2-(4-iodophenyl)benzamide (4.45 g, 0.0138 moles, preparation 56), acetonitrile (45 mL), and triethylamine (2.93 grams, 0.0289 moles) to a 100 mL 3-neck round-bottom flask equipped with a magnetic stirrer, internal temperature probe, ice-water bath, and addition funnel. Cool the contents of the 100 mL 3-neck round-bottom flask to 0° C. Add trifluoroacetic anhydride (3.04 grams, 0.0145 moles) to the reaction mixture via the addition funnel over 5 minutes. Observe a temperature increase to about 24° C., and cool the reaction mixture to 0° C. Stir the reaction mixture for 60 minutes. Add water (45 mL) and stir the suspension at ambient temperature for 60 minutes. Collect the precipitate by filtration and rinse the filter cake with water. Vacuum (15-25 mm) dry the filter cake at 50° C. to provide the title compound (4.03 g, 0.0132 moles) in 95.9% yield. 1H NMR(CDCl3, 500.0 MHz): δ 7.82 (app. d, 2H, J=9); 7.75 (dd, 1H, J=1.5, 8); 7.63 (dt, 1H, J=1.5, 7.5); 7.46 (d, 1H, J=8); 7.45 (dt, 1H, J=1.5, 7.5); 7.28 (app. d, 2H, J=8.5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625932B2
Source datasetuspto-grants-2009_12
ORD IDord-7cb3ed86102641878fdeb837087da598
Source noteuspto-grants-2009_12