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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270331Generated: October 28, 2026

4-(2-Piperidin-1-yl-ethoxy)benzyl chloride → 2-Methyl-2-(2-methyl-furan-3-sulfonyl)-3-[4-(2-piperidin-yl-ethoxy)-phenyl]-propionic acid ethyl ester

https://huagongshe.com/reaction/2270331

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Piperidin-1-yl-ethoxy)benzyl chlorideHCID 9860786—
Reactant2-(2-Methyl-furan-3-sulfonyl)-propionic acid ethyl esterHCID 53960737—
Product2-Methyl-2-(2-methyl-furan-3-sulfonyl)-3-[4-(2-piperidin-yl-ethoxy)-phenyl]-propionic acid ethyl esterHCID 53659048—

Reaction Steps

2-Methyl-2-(2-methyl-furan-3-sulfonyl)-3-[4-(2-piperidin-yl-ethoxy)-phenyl]-propionic acid ethyl ester was prepared according to the general method as outlined in example 9. Starting from 2-(2-methyl-furan-3-sulfonyl)-propionic acid ethyl ester (2.4 g, 9.8 mmol) and 1-[2-(4-chloromethylphenoxy)-ethyl]-piperidine (2.96 g, 10.7 mmol); Yield 2.4 g (92%); amber oil; MS 464.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06331563B1
Source datasetuspto-grants-2001_12
ORD IDord-a193e208a8994ca1867d0e72b1311b86
Source noteuspto-grants-2001_12