HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922592Generated: October 31, 2026
Trifluoroacetic acid → HCID 12271391, compound
https://huagongshe.com/reaction/922592
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Homoveratrylamine | HCID 8421 | — |
| Reactant | N-Iodosuccinamide | HCID 21864724 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 12271391 | HCID 12271391 | 70% |
Reaction Steps
To a solution of N-iodosuccinamide (NIS) (4.95 g, 22 mmol) in dry acetonitrile (50 mL) was added 2-(3,4-dimethoxyphenyl)ethanamine (3.32 mL, 20 mmol) and trifluoroacetic acid (3.85 mL, 50 mmol) with stirring. The mixture was stirred at room temperature in a 250 mL round bottom flask for two hours. The acetonitrile was removed and the remaining solid was taken up in water. The water solution was treated with saturated sodium bisulfite aqueous solution until the purple color disappeared. The pH was adjusted to 8 and the aqueous solution was extracted with dichloromethane (3×50 mL) The organic layers were combined and dried over sodium sulfate. The solvent was evaporated to yield 2-(2-iodo-4,5-dimethoxyphenyl)ethanamine (4.3 g, 70%). The crude product was dried under dynamic vacuum overnight and was sufficiently pure for subsequent steps.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278959B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-0202441a286c4d7db950922d446de677 |
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| Source note | uspto-grants-2016_03 |
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