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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587690Generated: October 29, 2026

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

https://huagongshe.com/reaction/587690

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 NaBH3CN (0.055 g, 0.875 mmol) in cooling and the reaction mixture was stirred at room temperature for 16 h. The reaction mixture was diluted with DCE, was washed with water and brine and dried over anhydrous Na2SO4. 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 numberUS09226501B2
Source datasetuspto-grants-2016_01
ORD IDord-df3bb7d86c7d48f383da7d9f825d770b
Source noteuspto-grants-2016_01