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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77696Erstellt: 23. Oktober 2026

3-(Trifluoromethyl)benzoyl chloride → N-(3-iodo-4-methylphenyl)-3-(trifluoromethyl)benzamide

https://huagongshe.com/de/reaction/77696

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
EduktDiisopropylethylamineHCID 81531—
Edukt3-Iodo-p-toluidineHCID 118889—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(3-iodo-4-methylphenyl)-3-(trifluoromethyl)benzamideHCID 792550692%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

To 3-iodo-4-methylaniline (500.0 mg, 2.145 mmol) was added dichloromethane (DCM) (10 mL) followed by N,N-diisopropylethylamine (DIPEA)(520 μL, 3.0 mmol) and 3-(trifluoromethyl)-benzoyl chloride (0.36 mL, 2.4 mmol). The reaction was stirred at 25° C. for 16 hours and was transferred to a separatory funnel and partitioned between water and dichloromethane (DCM). The organic phase was sequentially washed with 0.1N HCl, saturated aqueous NaHCO3, water, then saturated aqueous NaCl. The washed organic phase was then dried over MgSO4 and filtered and concentrated to leave the crude product. The crude product was triturated with hexanes to leave the product as an off-white solid, (797 mg, 92%). 1H NMR (400 MHz, CDCl3): δ 8.10 (m, 2H), 8.04 (d, 1H), 7.84 (bs, 1H), 7.81 (d, 1H), 7.63 (m, 1H), 7.58 (dd, 1H), 7.22 (d, 1H), 2.42 (s, 3H). MS (EI) m/z=274 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841318B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-8e1d154a8b984a23affefa947ae0cdfe
Quellennotizuspto-grants-2014_09