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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353514Generated: October 30, 2026

4-(4-But-2-ynyloxy-benzenesulfonyl)-1-(4-chloro-benzyl)-piperdine-4-carboxylic acid ethyl ester → 4-(4-But-2-ynyloxy-benzenesulfonyl)1-(4-chloro-benzyl)-piperdine-4-carboxylic acid

https://huagongshe.com/reaction/353514

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-But-2-ynyloxy-benzenesulfonyl)-1-(4-chloro-benzyl)-piperdine-4-carboxylic acid ethyl esterHCID 11752186—
SolventSodium HydroxideHCID 14798—
SolventMeOH tetrahydrofuranHCID 21899815—
Product4-(4-But-2-ynyloxy-benzenesulfonyl)1-(4-chloro-benzyl)-piperdine-4-carboxylic acidHCID 11271172—

Reaction Steps

4-(4-But-2-ynyloxy-benzenesulfonyl)-1-(4-chloro-benzyl)-piperdine-4-carboxylic acid was prepared starting from 4-(4-but-2-ynyloxy-benzenesulfonyl)-1-(4-chloro-benzyl)-piperdine-4-carboxylic acid ethyl ester (3.14 g, 6.42 mmol) dissolved in THF:methanol 3:1 (100 ml) and 10 N NaOH (10 ml). The resulting reaction mixture was worked up as outlined in Example 1 (Step 7). Yield 2.37 g (80%); white solid; mp 205° C.; MS: 461.9 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06753337B2
Source datasetuspto-grants-2004_06
ORD IDord-ba8e3df10b6847f29780f99d202a2b8e
Source noteuspto-grants-2004_06