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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502971Generated: October 30, 2026

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

https://huagongshe.com/reaction/1502971

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 numberUS09211281B2
Source datasetuspto-grants-2015_12
ORD IDord-92d7bcb222574db3ae7e8bc8b1bac010
Source noteuspto-grants-2015_12