Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515044Generated: November 2, 2026

Tetrafluoroboric acid → HCID 86651277, compound

https://huagongshe.com/reaction/1515044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrafluoroboric acidHCID 28118—
ReactantDiethyl vinylphosphonateHCID 69629—
Reactant4-Amino-2,6-dimethylbenzaldehydeHCID 12381235—
ReactantSodium NitriteHCID 23668193—
Catalystpalladium(II) acetateHCID 167845—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 86651277HCID 86651277—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Amino-2,6-dimethylbenzaldehyde (149 mg, 1.0 mmol)) was taken up in enough 42% HBF4 until the suspension stirred well and then was cooled to 0° C. To this was added a solution of NaNO2 (69 mg, 1.0 mmol) in water (0.5 mL) slowly. After 30 minutes at 0° C., MeOH (3 mL) was added and followed by Pd(OAc)2 (7.5 mg) and vinylphosphonic acid diethyl ester (197 mg, 1.2 mmol). The reaction mixture was heated at 80° C. for 30 min and the suspension was filtered through Celite, washed with CH2Cl2, and the filtrate was extracted with CH2Cl2. The organic layer was washed with water, brine, dried with MgSO4, and filtered. The solvent was removed under reduced pressure and the residue was purified by flash chromatography using heptane/EtOAc (4:1 then followed by 100% EtOAc) to give [(E)-2-(4-formyl-3,5-dimethylphenyl)-vinyl]-phosphonic acid diethyl ester as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222248B2
Source datasetuspto-grants-2012_07
ORD IDord-34f2fbabe198464291ff124aaba10a63
Source noteuspto-grants-2012_07