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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278291Generated: October 30, 2026

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

https://huagongshe.com/reaction/278291

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-But-2-ynyloxy-benzenesulfonyl)-1-(4-methoxy-benzyl)-piperidine-4-carboxylic acid ethyl esterHCID 11363756—
SolventSodium HydroxideHCID 14798—
SolventMeOH tetrahydrofuranHCID 21899815—
Product4-(4-But-2-ynyloxy-benzenesulfonyl)-1-(4-methoxy-benzyl)-piperdine-4 carboxylic acidHCID 11201935—

Reaction Steps

4-(4-But-2-ynyloxy-benzenesulfonyl)-1-(4-methoxy-benzyl)-piperdine-4-carboxylic acid was prepared starting from 4-(4-but-2-ynyloxy-benzenesulfonyl)-1-(4-methoxy-benzyl)-piperdine-4-carboxylic acid ethyl ester (2.5 g, 5.15 mmol) dissolved in THF:methanol (3:1, 200 ml) and 10 N NaOH (15 ml). The resulting reaction mixture was worked up as outlined in Example 1 (Step 7). Yield 1.26 g (54%); off white solid; mp 223° C.; MS: 458 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358980B1
Source datasetuspto-grants-2002_03
ORD IDord-380919609396454f9e85b55d6e57d8ce
Source noteuspto-grants-2002_03