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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251798Generated: October 27, 2026

6-Nitroveratraldehyde → HCID 178487640, compound

https://huagongshe.com/reaction/251798

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-NitroveratraldehydeHCID 88505—
ReactantPotassium FluorideHCID 522689—
ReactantHCID 13240488HCID 13240488—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventAcetonitrileHCID 6342—
ProductHCID 178487640HCID 17848764018%

Reaction Steps

4,5-Dimethoxy-2-nitrobenzaldehyde (1.52 g, 7.19 mmol), 353.0 mg (6.07 mmol) of potassium fluoride, and 134.8 mg (0.59 mmol) of benzyltriethylammonium chloride were added to a solution of 1.51 g (5.97 mmol) of phenylthio(trimethylsilyl)methyl isothiocyanate, synthesized according to a document (J. Chem. Soc., Perkin Trans 1 1984, 435.), in acetonitrile (36 ml), and the mixture was stirred at room temperature overnight. The solvent was removed from the reaction solution by distillation, and the water and chloroform were then added to the residue. The aqueous layer was extracted with chloroform. The organic layer was washed with saturated brine and was then dried over anhydrous sodium sulfate. The solvent was removed by distillation. The residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1→1:1) to give 302.4 mg (yield 18%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07867980B2
Source datasetuspto-grants-2011_01
ORD IDord-28be155f82dd4f2bb9d6b853b28f3c64
Source noteuspto-grants-2011_01