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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249626Generated: November 3, 2026

Acetic Anhydride → HCID 13340163, compound

https://huagongshe.com/reaction/1249626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 13340162HCID 13340162—
SolventEthyl AcetateHCID 8857—
ProductHCID 13340163HCID 1334016327%

Reaction Steps

A solution of 1.0 g. (0.0027 mole) of 3-acetoxy-2-methyl-6-[1-acetoxy-2-(N-tert-butylacetamido)ethyl]-pyridine N-oxide in 10 ml. of acetic anhydride was heated at the reflux temperature for 2.5 hours, then was allowed to cool to room temperature and stirred at this temperature overnight. The reaction mixture was poured into a two phase mixture of ethyl acetate and aqueous sodium bicarbonate and stirred for 1 hour. The organic layer was separated, dried over anhydrous magnesium sulfate, filtered and evaporated to dryness in vacuo to give a brown oil which was purified by column chromatography on silica gel with ether as the eluant to give 300 mg. (27%) of the desired product; m.p. 60°-64° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04632992
Source datasetuspto-grants-1986_12
ORD IDord-f9a8c63764514bde84c278cf8c105d37
Source noteuspto-grants-1986_12