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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29660Generated: October 26, 2026

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

https://huagongshe.com/reaction/29660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-tert-Butylbenzoyl chlorideHCID 74372—
ReactantMethyl 4-nitroanthranilateHCID 596476—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
Product2-(4-Tert-butyl-benzoylamino)-4-nitro-benzoic acid methyl esterHCID 6919452960%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420083B2
Source datasetuspto-grants-2008_09
ORD IDord-72ec1c9158684e528be265558f7462da
Source noteuspto-grants-2008_09