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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221632Generated: October 31, 2026

2-Oxime 2,3-butanedione → HCID 23076346, compound

https://huagongshe.com/reaction/2221632

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Oxime 2,3-butanedioneHCID 6398969—
ReactantMethyl 5-formyl-2-methylbenzoateHCID 19700886—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
ProductHCID 23076346HCID 2307634641%

Reaction Steps

A mixture of methyl 5-formyl-2-methylbenzoate (2.10 g), 2,3-butanedione-2-oxime (1.19 g) and 4N hydrogenchloride-ethyl acetate (50 mL) was stirred at room temperature for 3 days. The reaction mixture was concentrated, diethyl ether was added to the residue to allow precipitation of crystals, and crystals were collected by filtration. A mixture of the obtained crystal, tetrahydrofuran (50 mL) and thionyl chloride (2.11 g) was heated under reflux for 2 hrs. The reaction mixture was concentrated and ethyl acetate was added to the residue. The ethyl acetate layer was washed successively with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The obtained residue was subjected to silica gel column chromatography to give methyl 5-(4-chloromethyl-5-methyl-1,3-oxazol-2-yl)-2-methylbenzoate as colorless crystals (1.34 g, yield 41%) from a fraction eluted with ethyl acetate-hexane (1:9, v/v). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 89-90° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368578B2
Source datasetuspto-grants-2008_05
ORD IDord-f92ae9069d7146f892ced36c04bc8405
Source noteuspto-grants-2008_05