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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082712Generated: October 25, 2026

Ammonia → n-Propoxybenzamidine methyl sulfate

https://huagongshe.com/reaction/2082712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethyl 2-n-propoxybenzimidate methyl sulfateHCID 86735597—
SolventEthanolHCID 702—
Productn-Propoxybenzamidine methyl sulfateHCID 8673486760%

Reaction Steps

To a warm, stirred solution of 2-n-propoxybenzamide (896 g., 5.0 moles) in 1,2-dichloroethane (5 l) was added dimethyl sulfate (950 ml., 10.0 moles) over a period of about 0.5 hour. The mixture was stirred and heated under reflux for 17 hours. The solvent was removed. The residual oily solid was collected by filtration, washed with ethyl acetate and dried to give methyl 2-n-propoxybenzimidate methyl sulfate (403 g.), m.p. 79°-82°. The combined filtrate and washings were stored at 0° for 18 hours and gave a second crop (503 g.) of benzimidate, m.p. 81°-83°. A slurry of the methyl 2-n-propoxybenzimidate methyl sulfate (906 g.) in ethanol (1 l) was added to ethanol ( 4 l) which had previously been saturated with gaseous ammonia. The mixture was stored at room temperature for 17 hours. The mixture was filtered. The filtrate was evaporated to dryness to give 2-n-propoxybenzamidine methyl sulfate (872 g., 60%), m.p. 86°-88°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04082751
Source datasetuspto-grants-1978_04
ORD IDord-e062777e0e5245c9bd927f99545a8aa8
Source noteuspto-grants-1978_04