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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437426Generated: October 26, 2026

Triethyloxonium tetrafluoroborate → Ethyl 2-cyclopropylmethoxybenzimidate fluoroborate

https://huagongshe.com/reaction/437426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
Reactant2-(Cyclopropylmethoxy)benzamideHCID 2728029—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-cyclopropylmethoxybenzimidate fluoroborateHCID 8673487066%

Reaction Steps

A solution of triethyloxonium fluoroborate (99.1 g., 0.522 mole) in methylene chloride (225 ml.) was added to a stirred solution of 2-cyclopropylmethoxybenzamide (99.2 g., 0.518 mole) in methylene chloride (450 ml.). The mixture was stirred at 22° for 18 hours. The solution was concentrated to about one-fifth volume and then diluted with diethyl ether. The precipitated solid was recrystallized from methylene chloride - diethyl ether to give ethyl 2-cyclopropylmethoxybenzimidate fluoroborate (104.7 g., 65.7%), m.p. 120°-121°. To a stirred, cooled (ice-water) mixture of the fluoroborate (104.7 g.) in ethanol (100 ml.) was added 400 ml. of 6% ethanolic ammonia. The mixture was stirred for 18 hours at 20°. The mixture was concentrated and the residue partitioned between diethyl ether and 3N sodium hydroxide. The ether layer was washed with brine and dried over sodium sulfate. The dried solution was treated with hydrogen chloride. The precipitate was recrystallized from methylene chloride-diethyl ether to give 2-cyclopropylmethoxybenzamidine hydrochloride (71.5 g., 92.5% from fluoroborate), m.p. 166°-171°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031093
Source datasetuspto-grants-1977_06
ORD IDord-c7ebc9735906446fb01575c921fa1ec9
Source noteuspto-grants-1977_06