Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861887Generated: November 1, 2026

Tetrafluoroboric acid → HCID 15840530, compound

https://huagongshe.com/reaction/1861887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrafluoroboric acidHCID 28118—
ReactantHCID 15840529HCID 15840529—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
ProductHCID 15840530HCID 15840530—

Reaction Steps

In an ice bath, ethyl 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-3-aminonaphthalene-2-carboxylate (Compound C, 150 mg, 0.55 nmol) was added 0.24 ml of HBF4 (48% solution in water), followed by a solution of NaNO2 (81 mg, 1.16 mmol) in 1 ml of water. The slurry was left in a refrigerator for 3 days. The reaction mixture was washed successively with ethyl acetate until TLC showed no UV visible spot at the baseline. The ethyl acetate layer was dried with MgSO4 and the solution was concentrated to an oil. The oil was further dissolved in 1 ml of toluene and the mixture was heated under reflux for 2 h. After the reaction cooled to room temperature, solvent was evaporated and the residue was passed through a column (silica gel, ethyl acetate/hexane 1/10) to give the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06534544B1
Source datasetuspto-grants-2003_03
ORD IDord-f1c8ef829c0149968241415c50c2e9d1
Source noteuspto-grants-2003_03