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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383402Generated: October 25, 2026

5-Methyl-2-nitrobenzoic acid → Ethyl 2-(hydroxyimino)-2-(5-methyl-2-nitrobenzamido)acetate

https://huagongshe.com/reaction/383402

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methyl-2-nitrobenzoic acidHCID 18371—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 178472862HCID 178472862—
SolventAcetonitrileHCID 6342—
ProductEthyl 2-(hydroxyimino)-2-(5-methyl-2-nitrobenzamido)acetateHCID 13638871392.4%

Reaction Steps

To 5-methyl-2-nitro-benzoic acid (100 mg, 0.55 mmol), ethyl 2-(hydroxyamino)-2-imino-acetate (73 mg, 0.55 mmol), and HATU (210 mg, 0.55 mmol) were added acetonitrile (4 mL) and DIEA (96 μL, 0.55 mmol). The reaction was stirred at room temperature for 25 min resulting in a thick white precipitate. The solid was filtered, washed with water then dried to yield ethyl 2-(hydroxyimino)-2-(5-methyl-2-nitrobenzamido)acetate as a white solid (150 mg, 92% yield). LC/MS m/z 296.1 [M+H]+. 1H NMR (400.0 MHz, DMSO-do) δ 8.05 (d, J=8.3 Hz, 1H), 7.74 (d, J=0.9 Hz, 1H), 7.61 (d, J=8.4 Hz, 1H), 7.16 (br s, 2H), 4.28 (q, J=7.1 Hz, 2H), 2.47 (s, 3H), 1.28 (t, J=7.1 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367660B2
Source datasetuspto-grants-2013_02
ORD IDord-c0b6145d9eb140a4b930876ce69c9fd6
Source noteuspto-grants-2013_02