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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239789Generated: November 2, 2026

Dichloromethane → 1-((3-Methylbenzo[b]thiophen-2-yl)methyl)piperazine dihydrochloride

https://huagongshe.com/reaction/2239789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
Reactantt-Butyl 4-((3-methylbenzo[b]thiophen-2-yl)methyl)piperazine-1-carboxylateHCID 68415560—
Product1-((3-Methylbenzo[b]thiophen-2-yl)methyl)piperazine dihydrochlorideHCID 68413724—

Reaction Steps

The title A compound, t-butyl 4-((3-methylbenzo[b]thiophen-2-yl)methyl)piperazine-1-carboxylate is dissolved in dry DCM (50 mL), and 5 equiv. of TFA are added at 0° C. The reaction mixture is stirred at RT for 3 h. After the solvent is evaporated in vacuo, the residue is trituated in Et2O, and the precipitate that forms is collected by filtration, washed with EtOH and dried in a vacuum oven at 40° C. overnight to give a hygroscopic solid. The solid is treated with sodium bicarbonate solution, and extracted with EtOAc. The organic layer is evaporated in vacuo, and the residue is dissolved in Et2O and treated with a solution of hydrochloric acid in Et2O. The precipitated solid is collected by filtration and dried to give 1-((3-methylbenzo [b]thiophen-2-yl)methyl)piperazine dihydrochloride: LC/MS (M+1=247.1). 1H NMR (DMSO-d6, 200 MHz) δ 2.48 (s, 3H), 3.39 (m, 4H), 3.54 (m, 4H), 4.63 (s, 2H), 7.45 (m, 2H), 7.84 (d, 1H, J=7.2 Hz), 7.95 (d, 1H, J=7.2 Hz), 9.52 (br s, NH). Anal. calculated for (C14H18N2S 2HCl): C, 52.66; H, 6.31; Cl, 22.21; N, 8.77; S, 10.04. Found: C, 52.70; H, 6.58; N, 8.77; S, 9.70.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723343B2
Source datasetuspto-grants-2010_05
ORD IDord-56442da7b6d64b9487ef3bbbff457b4e
Source noteuspto-grants-2010_05