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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066497Generated: October 31, 2026

Triethyloxonium tetrafluoroborate → HCID 21200268, compound

https://huagongshe.com/reaction/1066497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
ReactantHCID 6461349HCID 6461349—
ReactantDichloromethane methanolHCID 21226129—
SolventDichloromethaneHCID 6344—
ProductHCID 21200268HCID 21200268—

Reaction Steps

Under an atmosphere of argon 11.36 g of 3-benzyloxybenzamide were suspended in CH2Cl2 (200 ml) and 9.5 g triethyloxonium fluoroborate in CH2Cl2 (100 ml) were added dropwise on ice cooling. The reaction mixture was then stirred further 20 h at RT until completion of reaction according to TLC analysis (CH2Cl2/MeOH: 15/1). The solid which had formed was filtered off, washed with ether to give the desired ethyl m-benzyloxybenzimidate tetrafluoroborate as white crystals, mp 152°-154° C., which was used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06242601B1
Source datasetuspto-grants-2001_06
ORD IDord-f0cc0210d5be42109de96a78f3e0b793
Source noteuspto-grants-2001_06