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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401012Generated: October 29, 2026

Hydrochloric Acid → HCID 51347929, compound

https://huagongshe.com/reaction/401012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantUreaHCID 1176—
Reactant3-Ethoxy-4-hydroxy-5-nitrobenzaldehydeHCID 584878—
Reactant2-(3,4-Difluorophenyl)-1-phenylethanoneHCID 2758317—
SolventEthanolHCID 702—
ProductHCID 51347929HCID 5134792943.4%

Reaction Steps

To a solution of 2-(3,4-difluorophenyl)-1-phenylethanone (Intermediate 12) (150 mg, 0.65 mmol), 3-ethoxy-4-hydroxy-5-nitrobenzaldehyde (128.1 mg, 0.65 mmol), and urea (117 mg, 1.95 mmol) in 20 mL of ethanol was added 0.2 ml con. HCl. The mixture was refluxed for 2 days. After the solvent was removed under reduced pressure, the residue was purified by reverse-phase preparatory HPLC (26-53% acetonitrile+0.1% trifluoroacetic acid in water+0.1% trifluoroacetic acid, over 15 min.) to give Compound 30 (132 mg, yield 43.3%). 1H NMR (DMSO-d6 400 MHz): δ 10.30 (s, 1H), 8.82 (s, 1H), 7.58 (s, 1H), 7.43 (s, 1H), 7.30-7.20 (m, 6H), 7.07 (m, 1H), 6.86 (m, 1H), 6.59 (s, 1H), 5.27 (s, 1H), 4.08 (m, 2H), 1.33 (t, J=6.8 Hz, 3H); MS (ESI): m/z 468.0 [M+1]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741915B2
Source datasetuspto-grants-2014_06
ORD IDord-defa1115958e4d81b879cce407547081
Source noteuspto-grants-2014_06