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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519590Generated: November 3, 2026

Sodium triacetoxyborohydride → 2,6-Difluoro-4-(2-{4-[2-(4-nitrophenyl)ethyl]piperazin-1-yl}ethyl)benzonitrile

https://huagongshe.com/reaction/1519590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2,6-Difluoro-4-(2-oxoethyl)benzonitrileHCID 10329945—
Reactant1-[2-(4-Nitrophenyl)ethyl]piperazineHCID 14985965—
SolventDichloromethaneHCID 6344—
Product2,6-Difluoro-4-(2-{4-[2-(4-nitrophenyl)ethyl]piperazin-1-yl}ethyl)benzonitrileHCID 68071665—

Reaction Steps

A solution of 2,6-difluoro-4-(2-oxoethyl)benzonitrile (185 mg, 1.0 mmol), 1-[2-(4-nitrophenyl)ethyl]piperazine (200 mg, 0.85 mmol) and NaBH(OAc)3 (720 mg, 3.4 mmol) in anhydrous DCM (10 mL) was stirred at ambient temperature overnight. The reaction was completed according to TLC. The reaction mixture was added 20 mL of DCM, washed with brine, separated the organic layer, dried over anhydrous sodium sulfate and concentrated. The residue was purified by preparative TLC to give the product. 1H-NMR (400 MHz, CDCl3) δ ppm 8.15˜8.17 (d, J=8.6 Hz, 2H), 7.37˜7.39 (d, J=8.6 Hz, 2H), 6.92˜6.94 (d, J=8.6 Hz, 2H), 2.50˜3.11 (m, 16H). MS m/z: 401 (M+1)+. (0.16 μM)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073882B2
Source datasetuspto-grants-2015_07
ORD IDord-98918b38b4f44c52817aa36508552e5b
Source noteuspto-grants-2015_07