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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701588Generated: October 25, 2026

N-Benzylformamide → Ethyl N-Benzylformimidate

https://huagongshe.com/reaction/1701588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-BenzylformamideHCID 80654—
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
SolventDichloromethaneHCID 6344—
ProductEthyl N-BenzylformimidateHCID 19022221—

Reaction Steps

A solution of 690 mg (5.1 mmoles) of N-benzylformamide in 5 ml of methylene chloride is cooled in an ice-water bath and put under an argon blanket. The solution is stirred while 4.9 ml (4.9 mmoles) of 1 M triethyloxonium fluoroborate in methylene chloride is added dropwise. After a 45 minute reaction time, the mixture is concentrated to dryness under reduced pressure at room temperature, and the residue is dried under reduced pressure over P2O5. The nuclear magnetic resonance spectrum of the product in deuterochloroform is fully in accord with the product being a fluoroborate etherate complex of ethyl N-benzylformimidate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04194047
Source datasetuspto-grants-1980_03
ORD IDord-db3c0f88c7884ec3acc461c5d9551a24
Source noteuspto-grants-1980_03