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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294607Generated: October 31, 2026

3,4-Dimethoxyphenyl methyl ketone → 1-[4-Chloro-3-(trifluoromethyl)phenyl]-4-[1-(3,4-dimethoxyphenyl)ethyl]piperazine

https://huagongshe.com/reaction/1294607

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dimethoxyphenyl methyl ketoneHCID 14328—
Reactant1-(4-Chloro-3-(trifluoromethyl)phenyl)piperazineHCID 2778137—
CatalystHCID 178460666HCID 178460666—
SolventMethanolHCID 887—
Product1-[4-Chloro-3-(trifluoromethyl)phenyl]-4-[1-(3,4-dimethoxyphenyl)ethyl]piperazineHCID 10137452—

Reaction Steps

A quantity of 0.17 g (0.6 mmole, 1 eq) of 1-(4-chloro-3-trifluoromethyl-phenyl)-piperazine and 0.1 g (0.6 mmole, 1 eq) of 3,4-dimethoxyacetophenone and 2 mL of Ti(OiPr)4 are warmed to 70° C. for 2 hours. The reaction solution is cooled to room temperature and 20 mL of anhydrous methanol is added followed by 1.0 g of NaBH and the resulting solution is stirred at room temperature for 2 hours. The reaction is quenched by the addition of 1 N NaOH and extracted with CH2Cl2. The CH2Cl2 extracts are dried over anhydrous MgSO4 and concentrated in vacuo. The residue is chromatographed on SiO2 with ethyl to afford 1-[4-chloro-3-(trifluoromethyl)phenyl]-4-[1-(3,4-dimethoxyphenyl)ethyl]piperazine (compound 2). Analysis 1H NMR (400 MHz, CDCl3): 7.31 (1H, d), 7.19 (1H, m), 6.90 (4H, m), 3.89 (6H, d), 3.38 (1H, m), 3.20 (4H, m), 2.61 (4H, m). MS (LC-MS): Calculated for C21H24ClF3N2O2 428.88. Found 429.30 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241765B2
Source datasetuspto-grants-2007_07
ORD IDord-c1ab1733162b4b65943b173d641382e0
Source noteuspto-grants-2007_07