Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828296Generated: October 30, 2026

1-(2-Fluorophenyl)piperazine → HCID 10064035, compound

https://huagongshe.com/reaction/1828296

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Fluorophenyl)piperazineHCID 70529—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDichloromethaneHCID 6344—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 10064035HCID 10064035—

Reaction Steps

1-(2-Fluorophenyl)piperazine (0.18 g, 1.0 mmol) and sodium triacetoxyborohydride (0.32 g, 1.5 mmol) in dichloroethane (2 mL) were treated with the product from Example 35B (2 mL, 1.0 mmol) as a 0.5M solution in dichloroethane dropwise. The mixture was allowed to stir at room temperature for 17 hours. The mixture was diluted with dichloromethane (10 mL) and washed with 1N NaOH. The organic layer was dried over magnesium sulfate, filtered, and the filtrate concentrated under reduced pressure. The residue was purified by flash chromatography on silica (dichloromethane to 2% methanol in dichloromethane) to provide the title compound. 1H NMR (CDCl3, 400 MHz) δ 2.81 (br, 4H), 3.19 (br, 4H), 3.85 (s, 2H), 6.89 (s, 1H), 7.00 (m, 4H), 7.20 (dd, J=4.75, 8.14 Hz, 1H), 7.74 (d, J=8.48 Hz, 1H), 8.52 (d, J=4.75 Hz, 1H); MS (DCI/NH3) m/z 312.2 (M+H)+; Anal. Calcd for C18H18FN3O: C, 69.44; H, 5.83; N, 13.50. Found: C, 69.36; H, 5.59; N, 13.28.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07057042B2
Source datasetuspto-grants-2006_06
ORD IDord-03b4ad7839084deabfba76f9fa1e7d7f
Source noteuspto-grants-2006_06