HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251798Generated: October 27, 2026
6-Nitroveratraldehyde → HCID 178487640, compound
https://huagongshe.com/reaction/251798
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Nitroveratraldehyde | HCID 88505 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | HCID 13240488 | HCID 13240488 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178487640 | HCID 178487640 | 18% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07867980B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-28be155f82dd4f2bb9d6b853b28f3c64 |
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| Source note | uspto-grants-2011_01 |
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