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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419546Generated: October 31, 2026

Sodium borohydride → 2-(Methyloxy)-4-(4-propyl-1-piperazinyl)aniline

https://huagongshe.com/reaction/419546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-[3-(Methyloxy)-4-nitrophenyl]-4-propylpiperazineHCID 59860266—
CatalystDichloronickel;hexahydrateHCID 11791229—
SolventMeOH tetrahydrofuranHCID 21899815—
Product2-(Methyloxy)-4-(4-propyl-1-piperazinyl)anilineHCID 5986028293.2%

Reaction Steps

A mixture of 1-[3-(methyloxy)-4-nitrophenyl]-4-propylpiperazine (0.204 g, 0.73 mmol) and nickel(II) chloride hexahydrate (0.087 g, 0.37 mmol) was stirred in 2:1 MeOH/THF (7 mL) under N2 at rt. To this mixture was added NaBH4 (0.097 g, 2.6 mmol) in 2 equal portions over 5 min. The reaction was stirred at rt for about 45 min, then concentrated under vacuum. The residue was dissolved in DCM and poured through Celite, washing with DCM and EtOAc. The filtrate was concentrated and chromatographed on silica gel to give the title compound of step B (170 mg, 0.68 mmol, 93%) as a grey oil. 1H NMR (400 MHz, DMSO-d6): δ 6.50 (d, 1H, J=8.25), 6.47 (d, 1H, J=2.38 Hz), 6.26 (dd, 1H, J=2.47 and 8.34 Hz), 4.19 (br s, 2H), 3.72 (s, 3H), 2.90-2.94 (m, 4H), 2.43-2.47 (m, 4H), 2.25 (t, 2H, J=7.42 Hz), 1.44 (q, 2H, J=7.39 Hz), 0.86 (t, 3H, J=7.33 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-e2d9e258f36c416592c274de253c04f0
Source noteuspto-grants-2012_01