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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419542Generated: November 1, 2026

Sodium borohydride → (2-(Ethyloxy)-4-[4-(1-methylethyl)-1-piperazinyl]phenyl}amine

https://huagongshe.com/reaction/419542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-[3-(Ethyloxy)-4-nitrophenyl]-4-(1-methylethyl)piperazineHCID 59452925—
CatalystDichloronickel;hexahydrateHCID 11791229—
SolventMeOH tetrahydrofuranHCID 21899815—
Product(2-(Ethyloxy)-4-[4-(1-methylethyl)-1-piperazinyl]phenyl}amineHCID 5945278593%

Reaction Steps

A mixture of 1-[3-(ethyloxy)-4-nitrophenyl]-4-(1-methylethyl)piperazine (0.285 g, 0.97 mmol) and nickel(II) chloride hexahydrate (0.116 g, 0.48 mmol) was stirred in 2:1 MeOH/THF (10 mL) under N2 at rt. To this mixture was added NaBH4 (0.129 g, 3.4 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 (238 mg, 0.90 mmol, 93%) as a grey oil. MS (ESI): 264 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-57603de864ea42a09709ce1157cdd1bd
Source noteuspto-grants-2012_01