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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29660Erstellt: 24. Oktober 2026

Triethylamine → 2-(4-Tert-butyl-benzoylamino)-4-nitro-benzoic acid methyl ester

https://huagongshe.com/de/reaction/29660

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt4-tert-Butylbenzoyl chlorideHCID 74372—
EduktMethyl 4-nitroanthranilateHCID 596476—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt2-(4-Tert-butyl-benzoylamino)-4-nitro-benzoic acid methyl esterHCID 6919452960%

Reaktionsschritte

To a solution of 4-nitro-anthranilic acid methyl ester (1.500 g, 7.4 mmol) in CH2Cl2 (200 mL) was added triethylamine (8 mL) and 4-tert-butyl benzoyl chloride and the reaction was stirred overnight at rt. It was then poured into brine, extracted with ethyl acetate, dried over MgSO4 and concentrated in vacuo. The residue was purified by flash chromatography using ethyl acetate/hexanes (20/80) to afford 2-(4-tert-butyl-benzoylamino)-4-nitro-benzoic acid methyl ester (1.841 g, 60%) as a yellow solid. mp=146.0-148.4° C.; mass spectrum (−ES, M−H) in/z 355. 1H NMR (400 MHz, DMSO-d6); δ 11.60 (bs, 1H), 9.35 (d, 1H), 8.20 (d, 1H), 8.02 (dd, 1H), 7.90 (d, 2H), 7.64 (d, 2H), 3.95 (s, 3H), 1.36 (s, 9H). Elemental analysis: Calcd. for C19H20N2O5: C, 64.04; H, 5.66; N, 7.86, Found: C, 64.04; H, 5.79; N, 7.76.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07420083B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-72ec1c9158684e528be265558f7462da
Quellennotizuspto-grants-2008_09