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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413074Generated: October 29, 2026

Chloroform → 2-Propyloxybenzamidine Hydrochloride

https://huagongshe.com/reaction/413074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-PropoxybenzonitrileHCID 2760470—
ReactantTriethylaluminumHCID 16682930—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
Product2-Propyloxybenzamidine HydrochlorideHCID 12254225—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

21.41 g (400 mmol) of ammonium chloride are suspended in 400 ml of toluene and cooled to 0-5° C. 200 ml of a 2M solution of triethylaluminium in hexane are added dropwise, and the mixture is stirred at room temperature until the evolution of gas has ceased. After addition of 32.2 g (200 mmol) of 2-propoxybenzonitrile, the reaction mixture is stirred at 80° C. (bath) overnight. With ice-cooling, the cooled reaction mixture is added to a suspension of 300 g of silica gel and 2.85 of ice-cooled chloroform, and the mixture is stirred for 30 minutes. The mixture is filtered off with suction and the filter residue is washed with the same amount of methanol. The solvent is distilled off under reduced pressure, the residue is stirred with 500 ml of a mixture of dichloromethane and methanol (9:1), the solid is filtered off and the mother liquor is concentrated. The residue is stirred with petroleum ether and filtered off with suction. This gives 22.3 g (52%) of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06566360B1
Source datasetuspto-grants-2003_05
ORD IDord-2d3bcf1612ca4dd4814b40754298ed34
Source noteuspto-grants-2003_05