Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568725Generated: October 26, 2026

Benzene → N-(3,4-dihydro-6-methoxy-2,5,7,8-tetramethyl-2H-benzopyran-2-yl)-acetylguanidine

https://huagongshe.com/reaction/568725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantGuanidineHCID 3520—
ReactantThionyl ChlorideHCID 24386—
Reactant(3,4-dihydro-6-methoxy-2,5,7,8-tetramethyl-2H-benzopyran-2-yl)acetic acidHCID 14210610—
CatalystDimethylformamideHCID 6228—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductN-(3,4-dihydro-6-methoxy-2,5,7,8-tetramethyl-2H-benzopyran-2-yl)-acetylguanidineHCID 86742025—

Reaction Steps

To a solution composed of 8.82 g (31.7 mmol) of (3,4-dihydro-6-methoxy-2,5,7,8-tetramethyl-2H-benzopyran-2-yl)acetic acid, 5.66 g of thionyl chloride and 20 ml of benzene was added 2 drops of N,N-dimethylformamide, and the mixture was refluxed for 2 hours. Low-boiling substances were distilled off from the reaction mixture under reduced pressure. The residue was dissolved in 20 ml of dioxane and the solution was added dropwise to a solution composed of 65 millimoles of guanidine, 7.5 ml of ethanol and 25 ml of dioxane at room temperature. Thereafter, the resultant mixture was stirred at room temperature for 1 hour and so obtained reaction mixture was poured into water and extracted with diethyl ether. The ether extract was washed with a saturated aqueous solution of sodium chloride and then dried over anhydrous sodium sulfate. Low-boiling substances were distilled off under reduced pressure. The residue was purified by silica gel column chromatography and recrystallized from methylene chloride/diethyl ether/n-hexane to give 5.1 g of N-(3,4-dihydro-6-methoxy-2,5,7,8-tetramethyl-2H-benzopyran-2-yl)-acetylguanidine [Compound (1)], which shows the following physical characteristics.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04728650
Source datasetuspto-grants-1988_03
ORD IDord-3a7d57c7cac949ea90a3950c4d873126
Source noteuspto-grants-1988_03