Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465154Generated: October 26, 2026

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

https://huagongshe.com/reaction/1465154

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 a solution of 5-methyl-2-nitro-benzoic acid (100 mg, 0.55 mmol) and HATU (210 mg, 0.55 mmol) in acetonitrile (4 mL) and DIEA (96 μL, 0.55 mmol) was added ethyl 2-(hydroxyamino)-2-imino-acetate (73 mg, 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 and 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-d6) 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 numberUS08999976B2
Source datasetuspto-grants-2015_04
ORD IDord-9c5d0a21a56c4165a8e9c9f37004d460
Source noteuspto-grants-2015_04