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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068624Generated: October 30, 2026

Oxalic acid dihydrate → HCID 21189943, compound

https://huagongshe.com/reaction/1068624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalic acid dihydrateHCID 61373—
ReactantHCID 21190027HCID 21190027—
SolventHydrochloric AcidHCID 313—
SolventSodium HydroxideHCID 14798—
ProductHCID 21189943HCID 2118994331.9%

Reaction Conditions

Temperature62.5 °C

Reaction Steps

A mixture of 1,2-diamino-4-bromo-6-ethylbenzene (40 mg, 0.14 mmol) and oxalic acid dihydrate (25 mg, 0.20 mmol, used as received) in 4 N HCl (1.5 mL) was refluxed at 120-5° C. for 3 h, then cooled to room temperature. The mixture was centrifuged and the liquid layer was removed. The yellow solid was washed with cold water (2×1 mL), collected by filtration, and dried at 60° C. under reduced pressure for 2 h, affording 40 mg of crude product (80%) as a yellow powder. The crude product was dissolved in 1N NaOH (2 mL) and filtered. The filtrate was acidified to pH=5, affording 12 mg of pure title compound; mp: >350° C. (dec. from 300° C.), IR (KBr, cm−1):3410, 3164, 2919, 1740, 1705, 1600. 1H NMR (DMSO-d6): 1.099 (t, 3 H; J=6 Hz), 2.741 (q, 2 H, J=7.2 Hz), 7.117, (d, 1 H, J=1.8 Hz), 7.138 (d, 1 H, J=1.8 Hz); 11.343 (s, 1H); 11.958 (s, 1H). HRMS: calcd for C10H9BrN2O2 (M+) m/z: 267.9846; found 267.9853.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251903B1
Source datasetuspto-grants-2001_06
ORD IDord-618f70d7d39b4a93ba71fe33717bb1f7
Source noteuspto-grants-2001_06