Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305914Generated: November 3, 2026

1-Benzyl-4-[4-(4-chloro-phenoxy)-benzenesulfonyl]-piperidine-4-carboxylic acid ethyl ester → 4-[4-(4-Chlorophenoxy)benzenesulfonyl]-1-benzylpiperidine-4-carboxylic acid

https://huagongshe.com/reaction/2305914

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-[4-(4-chloro-phenoxy)-benzenesulfonyl]-piperidine-4-carboxylic acid ethyl esterHCID 10973288—
SolventSodium HydroxideHCID 14798—
Product4-[4-(4-Chlorophenoxy)benzenesulfonyl]-1-benzylpiperidine-4-carboxylic acidHCID 11733621—

Reaction Steps

1-Benzyl-4-[4-(4chloro-phenoxy)-benzenesulfonyl]-piperidine-4-carboxylic acid was prepared starting from 1-benzyl-4-[4-(4chloro-phenoxy)-benzenesulfonyl]-piperidine-4-carboxylic acid ethyl ester (2.11 g, 4.1 mmol) dissolved in TBF:methanol (3:1 150 ml) and 10 N NaOH (20 ml). The resulting reaction mixture was worked up as outlined in example 83. Yield 1.11 g (56%); white solid; mp 201° C.; MS: 485.9 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441023B1
Source datasetuspto-grants-2002_08
ORD IDord-221758dfdd71452cb21819f5a6f5140e
Source noteuspto-grants-2002_08