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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 984693Erstellt: 25. Oktober 2026

2-Iodotoluene → N-acetyl-o-toluidine

https://huagongshe.com/reaction/984693

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-IodotolueneHCID 5128—
EduktN,N'-DimethylethylenediamineHCID 8070—
EduktPotassium FluorideHCID 522689—
EduktN,O-bis(trimethylsilyl)acetamideHCID 6913588—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelTolueneHCID 1140—
ProduktN-acetyl-o-toluidineHCID 844352%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

A Schlenk tube was charged with CuI (9.6 mg, 0.050 mmol, 5.0 mol %), KF (350 mg, 6.0 mmol), evacuated, backfilled with Ar. N,N′-Dimethylethylenediamine (11 μL, 0.10 mmol, 10 mol %), 2-iodotoluene (128 μL, 1.01 mmol), N,O-bis(trimethylsilyl)acetamide (300 μL, 1.21 mmol), and toluene (1.0 mL) were added under Ar. The Schlenk tube was sealed with a Teflon valve and the reaction mixture was stirred at 110° C. for 16 h. The resulting suspension was allowed to reach room temperature and then filtered through a 0.5×1 cm pad of silica gel eluting with ethyl acetate (20 mL). The filtrate was concentrated and the residue was purified by flash chromatography on silica gel (2×15 cm; hexane-ethyl acetate 1:4; 15 mL fractions). Fractions 10-17 provided 78 mg (52% yield) of N-(2-methylphenyl)acetamide as white needles.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06867298B2
Quelldatensatzuspto-grants-2005_03
ORD IDord-6fed5fec8902484fbd9c1448f51a015e
Quellennotizuspto-grants-2005_03