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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401010Generated: October 29, 2026

Hydrochloric Acid → HCID 51347779, compound

https://huagongshe.com/reaction/401010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantUreaHCID 1176—
Reactant2-(2-Chlorophenyl)-1-phenylethan-1-oneHCID 93681—
Reactant3-Ethoxy-4-hydroxy-5-nitrobenzaldehydeHCID 584878—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 51347779HCID 513477797%

Reaction Steps

To a mixture of 2-(2-chlorophenyl)-1-phenylethanone (Intermediate 10) (85 mg, 0.37 mmol), 3-ethoxy-4-hydroxy-5-nitrobenzaldehyde (94 mg, 0.45 mmol), and urea (67 mg, 1.1 mmol) in anhydrous EtOH (20 mL) was added concentrated HCl solution (0.1 mL), and the reaction mixture was refluxed for three days. TLC (EtOAc:MeOH=10:1) showed that about 50% of starting materials were consumed, and the reaction mixture was concentrated. The residue was purified by column chromatography (EtOAc:MeOH=40:1) and preparative HPLC to afford Compound 28 as a yellow solid (12 mg, yield: 7.0%). 1H NMR (CD3OD 400 MHz): δ 7.47 (s, 1H), 7.34-7.40 (m, 1H), 7.20 (s, 5H), 7.10-7.13 (m, 1H), 7.05 (s, 1H), 6.80-6.87 (m, 1H), 6.40-6.45 (m, 1H), 5.45 (s, 1H), 3.95-4.10 (m, 2H), 1.37-1.42 (m, 3H); MS (ESI): m/z 466.2 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741915B2
Source datasetuspto-grants-2014_06
ORD IDord-4023290732394934a59e0a1fc3826456
Source noteuspto-grants-2014_06