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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079142Generated: October 30, 2026

Tetrafluoroborate → HCID 72312817, compound

https://huagongshe.com/reaction/2079142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrafluoroborateHCID 26255—
ReactantProton spongeHCID 88675—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 72312794HCID 72312794—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 72312817HCID 7231281751%

Reaction Steps

After dissolving 322 mg of [2-(3-hydroxymethyl-4,5-dimethoxyphenyl) -2-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylimino]-1-methylsulfanylethylidene]carbamic acid methyl ester in 5 ml of dichloromethane, 364 mg of 1,8-bis(dimethylamino)naphthalene and 240 mg of Me3O+BF4− ere added and the mixture was stirred at room temperature for 5 hours. Saturated aqueous sodium hydrogencarbonate was added to the reaction mixture and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, the desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give the title compound (169 mg, isomeric mixture) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928228B2
Source datasetuspto-grants-2011_04
ORD IDord-703c135c20b74abc85d905c9a717298b
Source noteuspto-grants-2011_04