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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218107Generated: November 3, 2026

Dimethylformamide → 3-Benzyloxy-6-methyl-4-oxo-4H-pyran-2-carboxylic acid cyclohexylamide

https://huagongshe.com/reaction/2218107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantCyclohexylamineHCID 7965—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant6-Methyl-4-oxo-4H-pyran-2-carboxylic acidHCID 422942—
Product3-Benzyloxy-6-methyl-4-oxo-4H-pyran-2-carboxylic acid cyclohexylamideHCID 8661179761%

Reaction Steps

1,1′-carbonyldiimidazole (1.99 g, 12.30 mmol) was added to a solution of the 3-(benzyloxy,-6-methyl-4-oxo-4H-pyran-2-carboxylic acid (2.0 g, 7.69 mmol) in dimethylformamide (DMF, 18 ml) at room temperature. The resulting solution was heated at 40°-50° C. for 3 hrs. A light yellow solution was observed. Cyclohexylamine (1.23 ml, 10.76 mmol) was then added. The resulting mixture was stirred at room temperature for overnight. The DMF was removed under reduced pressure to give light yellow oil as a crude product, which was purified by flash column chromatography (elution gradient: from 1:1 ethyl acetate/hexane to 10% methanol in ethyl acetate) to yield the titled compound (1.60 g, yield 61%) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07410985B2
Source datasetuspto-grants-2008_08
ORD IDord-6feb1049c93c433aa74c70ecf8a045e3
Source noteuspto-grants-2008_08