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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595623Generated: November 1, 2026

HCID 11813035, compound → HCID 21704904, compound

https://huagongshe.com/reaction/1595623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11813035HCID 11813035—
ReactantMeOH tetrahydrofuranHCID 21899815—
SolventSodium HydroxideHCID 14798—
ProductHCID 21704904HCID 21704904—

Reaction Steps

1-(4-Bromo-benzyl)-4-(methoxy-benzenesulfonyl)-piperidine-4-carboxylic acid was prepared starting from 1-(4-bromo-benzyl)-4-(4-methoxy-benzenesulfonyl)-piperidine-4-carboxylic acid ethyl ester (16.5 g, 33.3 mmol) dissolved in THF:methanol 3:1 and 10 N NaOH (20 ml). The resulting reaction mixture was worked up as outlined in example 83. Yield 6.18 g (40%); tan solid; mp 215° C.; MS: 469.7 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288086B1
Source datasetuspto-grants-2001_09
ORD IDord-9d9490ac67204c31ae7a3538119b38e3
Source noteuspto-grants-2001_09