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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348998Generated: October 27, 2026

Methyl 6-methylnicotinate 1-oxide → Methyl 6-(acetoxymethyl)nicotinate

https://huagongshe.com/reaction/348998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 6-methylnicotinate 1-oxideHCID 15883477—
SolventAcetic AnhydrideHCID 7918—
ProductMethyl 6-(acetoxymethyl)nicotinateHCID 10353032121.2%

Reaction Steps

To a solution of methyl 6-methylnicotinate (6.05 g) in methylene chloride (100 mL) was added m-chloroperbenzoic acid (77%, 13.5 g). The reaction mixture was stirred at room temperature for 2 h and then diluted with chloroform (100 mL). The mixture was washed successively with aqueous sodium sulfite, saturated sodium bicarbonate, and brine. The organic later was then dried (sodium sulfate), filtered, and concentrated under reduced pressure to provide 6.21 g of methyl 6-methylnicotinate 1-oxide. A solution of methyl 6-methylnicotinate 1-oxide (4.35 g) in acetic anhydride (50 mL) was heated at 120° C. for 2 h and then concentrated under reduced pressure. Purification by flash column chromatography (silica gel, 1:2 to 3:5 ethyl acetate/hexanes) provided 3.3 g of the title compound: 1H NMR (300 MHz, CDCl3) δ 9.18, 8.31, 7.44, 5.29, 3.96, 2.19.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176242B2
Source datasetuspto-grants-2007_02
ORD IDord-aeb2713e5cf54385b03239a355fe75c8
Source noteuspto-grants-2007_02