HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520034Generated: November 4, 2026
3,3,3-Trifluoropropanal → 4-(4-Nitrophenyl)-1-(3,3,3-trifluoropropyl)-1,2,3,6-tetrahydropyridine
https://huagongshe.com/reaction/1520034
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,3,3-Trifluoropropanal | HCID 68028 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 4-(4-Nitrophenyl)-1,2,3,6-tetrahydropyridine | HCID 22048783 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 4-(4-Nitrophenyl)-1-(3,3,3-trifluoropropyl)-1,2,3,6-tetrahydropyridine | HCID 67984632 | 45.3% |
Reaction Steps
Sodium triacetoxyborohydride (6.2 g, 29.4 mmol, 2 eq.) was added to a solution of 4-(4-nitrophenyl)-1,2,3,6-tetrahydropyridine (3.0 g; 14.7 mmol; 1.0 eq.), DIEA (2.5 mL; 14.7 mmol; 1.0 eq.) and 3,3,3-Trifluoropropanal (2.4 mL; 29.4 mmol; 2.0 eq.) in DCE (60 mL). The reaction mixture was heated at 50° C. for 2 h and quenched by addition of a saturated solution of NH4Cl (50 mL). The phases were separated and organic phase was washed with water, dried over magnesium sulfate, filtered and concentrated to give a brown crude. Purification by flash chromatography on silica (EtOAc:heptane) afforded the title compound as a yellow solid (2.0 g, 45%). UPLC/MS: (MS+) 301.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073892B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-85a648b812dc4c6cbac6b082de4a6cb1 |
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| Source note | uspto-grants-2015_07 |
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