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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850293Generated: October 30, 2026

Ethanone, 2-(4-chlorophenyl)-1-phenyl- → HCID 85675368, compound

https://huagongshe.com/reaction/850293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanone, 2-(4-chlorophenyl)-1-phenyl-HCID 95829—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
SolventPyridineHCID 1049—
ProductHCID 85675368HCID 8567536892%

Reaction Steps

To a solution of 2-(4-chlorophenyl)-1-phenyl-1-ethanone (2, 1.93 g, 8.37 mmol) in 25 ml pyridine (dried over molecular sieves) under nitrogen was added at room temperature methoxylamine hydrochloride (873 mg, 10.5 mmol). The resulting slightly cloudy, pale orange mixture was stirred at room temperature overnight. The pyridine was removed in vacuo with heating. The residual solids were stirred with ether (60 ml), isolated by filtration, and discarded. The filtrate was dried over sodium sulfate, and concentrated in vacuo to give a mixture of the oxime geometrical isomers as 2.00 g of a clear, pale yellow syrup (92% yield). 1H NMR showed the isomers to be formed in a 5:3 ratio: Rf 0.64, 0.50; IR (CDCl3) 3068 (w), 2940 (m), 2819 (w), 1602 (w), 1493 (s), 1442 (m); 1H NMR (CDCl3) 7.63 (m, 2H), 7.37-7.11 (m, 11.5 H), 4.12 (s, 2H), 4.05 (s, 3H), 3.91 (s, 1.6H), 3.82 (s, 1.2H); low resolution mass spec. 259 (M+, 8), 227 (100), 192 (28), 165 (18), 134 (12), 125 (62), 119 (37).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017910
Source datasetuspto-grants-2000_01
ORD IDord-92098f08b7534645a60231142a86b7a4
Source noteuspto-grants-2000_01