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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161414Generated: October 30, 2026

Tetrafluoroborate → HCID 72312817, compound

https://huagongshe.com/reaction/1161414

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 were 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 numberUS07816522B2
Source datasetuspto-grants-2010_10
ORD IDord-2f6fe60b557a4356b90dd7ffe37ee4e2
Source noteuspto-grants-2010_10