Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419541Generated: October 26, 2026

Acetic Acid → 1-[3-(Ethyloxy)-4-nitrophenyl]-4-(1-methylethyl)piperazine

https://huagongshe.com/reaction/419541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetoneHCID 180—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1-(3-Ethoxy-4-nitrophenyl)piperazineHCID 59452580—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product1-[3-(Ethyloxy)-4-nitrophenyl]-4-(1-methylethyl)piperazineHCID 5945292588%

Reaction Steps

A mixture of 1-[3-(ethyloxy)-4-nitrophenyl]piperazine (Example 143, step A) (0.285 g, 1.13 mmol)) and acetone (0.13 g, 2.26 mmol) was stirred in DCE (5 mL) at rt under N2. To this mixture was added sodium triacetoxyborohydride (0.60 g, 2.8 mmol) and HOAc (0.136 g, 2.26 mmol). The reaction was stirred for approximately 24 h. The reaction was diluted with DCM and aqueous (saturated) NaHCO3. The aqueous layer was extracted with DCM (2×). The combined organic layers were dried over MgSO4, filtered, concentrated, and chromatographed on silica gel to give the title compound of step A (291 mg, 0.99 mmol, 88%) as a yellow solid. MS (ESI): 294 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-27928e72e31643b3bacc1bac412b06e5
Source noteuspto-grants-2012_01