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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762391Generated: November 2, 2026

Methanol → HCID 178437965, compound

https://huagongshe.com/reaction/1762391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant4-DimethylaminoacetophenoneHCID 75037—
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
ReactantHCID 70352008HCID 70352008—
SolventDichloromethaneHCID 6344—
ProductHCID 178437965HCID 178437965—

Reaction Steps

380 mg (2 mmol) of triethyloxonium tetrafluoroborate are dissolved in 15 ml of methylene chloride. 326 mg (2 mmol) of p-dimethylaminoacetophenone are added thereto at -15°. After 5 minutes there are added thereto at the same temperature 162 mg (1 mmol) of 1,3-diamino-2-ethyl-imidazolium chloride and the mixture is stirred at -10° for 1 hour and at 0° for 2 hours. After the addition of a small amount of methanol the mixture is evaporated and the residue is placed on a column loaded with 10 g of silica gel. The product is eluted with chloroform/methanol (87:13 parts by weight) and crystallized using ether. The crystallizate is dissolved in 80 ml of water, placed on a column loaded with ion exchanger Amberlite IRA 400 (chloride) and elution is carried out with water. The eluate is evaporated and the residue is crystallized from ethanol/water. There is obtained 3-amino-1-[[p-(dimethylamino)-α-methylbenzylidene]amino]-2 -ethylimidazolium chloride of melting point 223°-225°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04831151
Source datasetuspto-grants-1989_05
ORD IDord-3feb472eedf24981953d8ecf6f8a50b8
Source noteuspto-grants-1989_05