HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955132Generated: November 3, 2026
Veratraldehyde → 3,4-Dimethoxyphenylethanolamine
https://huagongshe.com/reaction/1955132
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Veratraldehyde | HCID 8419 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Catalyst | zinc(II)iodide | HCID 9883512 | — |
| Solvent | Nitromethane | HCID 6375 | — |
| Product | 3,4-Dimethoxyphenylethanolamine | HCID 3863978 | 54.8% |
Reaction Steps
To a stirred solution of veratraldehyde(16.6 g) and zinc iodide (50 mg) in anhydrous nitromethane (200 ml) was added trimethylsilyl cyanide (12 g) dropwise under nitrogen. After the resulting mixture was stirred at room temperature for 1 hour, the solvent was removed under reduced pressure. Anhydrous tetrahydrofuran (50 ml) was added to the residue, and the resulting mixture was added under ice cooling to a suspension of lithium aluminum hydride (3.9 g) in anhydrous tetrahydrofuran (200 ml). After that, the resulting mixture was stirred for 1 hour at room temperature. Water was added to the reaction mixture, insoluble matter was filtered off, and the solvent was then removed under pressure from the filtrate. Chloroform (300 ml) was added to the residue. The resulting mixture was washed with water and was then dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure. The thus-obtained residue was purified by a silica gel column, whereby the title compound (10.8 g, yield: 54.8%) was obtained as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06124347 |
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| Source dataset | uspto-grants-2000_09 |
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| ORD ID | ord-eb699b1906a642e2adf1075cac67a9f2 |
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| Source note | uspto-grants-2000_09 |
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