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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416623Generated: October 26, 2026

Acetic Acid → HCID 178522384, compound

https://huagongshe.com/reaction/416623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-Nitrobenzoyl chlorideHCID 8502—
ReactantSodium CarbonateHCID 10340—
Reactant3-Amino-4-hydroxypyridineHCID 233392—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 178522384HCID 17852238462%

Reaction Steps

A solution of p-nitrobenzoyl chloride (4.8 g, 25.7 mmol) in pyridine (77.0 mL) was added dropwise to a solution of 3-amino-4-hydroxypyridine (3.4 g, 30.9 mmol) in pyridine (51.0 mL) at 10° C. and stirred overnight. A solution of Na2CO3 (1.7 g) in water (65 mL) was added and the resultant mixture was stirred for 1 h. The reaction mixture was neutralized with 10% AcOH. The precipitate was collected by filtration, washed with 10% AcOH, and dried in vacuo (50° C.) to afford N-(4-hydroxypyridin-3-yl)-4-nitrobenzamide as a light green powder (4.1 g, Yield: 62%). 1HNMR (400 MHz, DMSO-d6) δ: 11.64 (1H, br s), 9.57 (1H, s), 9.07 (1H, s), 8.75 (1H, d, J=4.4 Hz), 8.36 (1H, d, J=8.8 Hz), 8.20 (1H, d, J=8.8 Hz), 7.74 (1H, d, J=4.4 Hz), 6.33 (1H, s); MS (ESI) calcd for C12H9N3O (m/z): 211. found: 212 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088928B2
Source datasetuspto-grants-2012_01
ORD IDord-8975606000cc48ce94900984d8c1c232
Source noteuspto-grants-2012_01