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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502832Generated: October 30, 2026

3,3,3-Trifluoropropylamine → HCID 86675154, compound

https://huagongshe.com/reaction/1502832

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3,3-TrifluoropropylamineHCID 10001—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 86675155HCID 86675155—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 86675154HCID 86675154—

Reaction Steps

To a stirred solution of (E)-5-(3-(3,5-dichloro-4-fluorophenyl)-4,4,4-trifluorobut-1-enyl)-2,3-dihydro-1H-inden-1-one (0.15 g, 0.35 mmol) in DCE (10 mL), was added trifluoropropyl amine (0.048 g, 0.42 mmol) and sodium cyanoborohydride (0.055 g, 0.875 mmol) in cooling and the reaction mixture was stirred at ambient temperature for 16 h. The reaction mixture was diluted with DCE, was washed with water and brine and dried over anhydrous sodium sulfate. Concentration under reduced pressure gave the crude compound, which was purified by flash column chromatography (SiO2, 100-200 mesh; 10-15% EtOAc in petroleum ether) to afford the title compound as a colorless gummy material (0.042 g, 24%): 1H NMR (400 MHz, CDCl3) δ 7.38-7.20 (m, 5H), 6.62 (d, J=16.0 Hz, 1H), 6.34 (dd, J=16.0, 8.0 Hz, 1H), 5.83 (br, 1H), 5.52 (m, 1H), 4.12 (m, 1H), 3.02 (m, 3H), 2.82 (m, 1H), 2.50 (m, 2H), 1.82 (m, 1H), 1.42 (m, 1H); ESIMS m/z 497.98 ([M−H]−); IR (thin film) 3027, 1654, 815 cm−1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09211280B2
Source datasetuspto-grants-2015_12
ORD IDord-7328c41f403648a2bd5059eebb213e64
Source noteuspto-grants-2015_12