HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374639Generated: October 29, 2026
Acetic Acid → Benzenemethanamine, N-butyl-2-fluoro-4-(trifluoromethyl)-
https://huagongshe.com/reaction/2374639
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | 2-Fluoro-4-(trifluoromethyl)benzaldehyde | HCID 522929 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzenemethanamine, N-butyl-2-fluoro-4-(trifluoromethyl)- | HCID 68855369 | 26% |
Reaction Steps
To a solution of 2-fluoro-4-(trifluoromethyl)benzaldehyde (3.84 g, 20.0 mmol) and n-butylamine (1.46 g, 20.0 mmol) in methanol (100 mL) were added acetic acid (4.6 mL, 80 mmol) and sodium cyanoborohydride (1.51 g, 24.0 mmol) and the solution was stirred at room temperature for 3 days. Water (10 mL) was added and the mixture was concentrated in vacuo. The residue was taken, up in aqueous 1 M KOH (125 mL) and ethyl acetate (100 mL) and the phases were separated. The aqueous phase was extracted with ethyl acetate (2×100 mL) and the combined organic phase was dried over Na2SO4 and concentrated in vacuo. Purification on a prepacked column of silica gel (Isolute® SPE Column, 70 g/150 mL) with ethyl acetate (33-100% gradient) in heptane as the eluent and collection of pure fractions yielded 1.28 g (26%) of a colourless oil of low viscosity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07462644B2 |
|---|
| Source dataset | uspto-grants-2008_12 |
|---|
| ORD ID | ord-54625a7efccb40a4b4839b6826077ed8 |
|---|
| Source note | uspto-grants-2008_12 |
|---|