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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3,3-TrifluoropropanalHCID 68028—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(4-Nitrophenyl)-1,2,3,6-tetrahydropyridineHCID 22048783—
Solvent1,2-DichloroethaneHCID 11—
Product4-(4-Nitrophenyl)-1-(3,3,3-trifluoropropyl)-1,2,3,6-tetrahydropyridineHCID 6798463245.3%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073892B2
Source datasetuspto-grants-2015_07
ORD IDord-85a648b812dc4c6cbac6b082de4a6cb1
Source noteuspto-grants-2015_07