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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807402Generated: October 30, 2026

Pyridine → HCID 86669076, compound

https://huagongshe.com/reaction/1807402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
ReactantHCID 67086633HCID 67086633—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 86669076HCID 8666907695.4%

Reaction Steps

To a stirred solution of trans 1-[2-(2,4,5-trichloro-thiophen-3-yl)-cyclopropyl]-ethanone (2.7 g; 10 mmol) prepared as described in example P29, in methanol (20 ml) at ambient temperature was added pyridine (1.25 ml; 15 mmol) and methoxyamine hydrochloride (1.3 g; 15 mmol). The reaction mixture was stirred for 4 hours at ambient temperature then poured in water (50 ml) and extracted with dichloromethane (3×30 ml). Combined organic layers were washed with water (30 ml) and dried over anhydrous sodium sulphate. The solvent was removed in vacuo to afford 2.85 g (95% of theory) of trans 1-[2-(2,4,5-trichloro-thiophen-3-yl)-cyclopropyl]-ethanone O-methyl-oxime as an E/Z mixture in form of an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357635B2
Source datasetuspto-grants-2013_01
ORD IDord-849cfcd667ee4fff9ddd86eeabf918ed
Source noteuspto-grants-2013_01