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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249701Generated: October 29, 2026

p-Toluenesulfonate → Methyl p-toluenesulfonate

https://huagongshe.com/reaction/249701

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-ToluenesulfonateHCID 85570—
ReactantKD-3010HCID 16048651—
ProductMethyl p-toluenesulfonateHCID 6645—
Productp-ToluenesulfonateHCID 85570—

Reaction Steps

The methyl ester precursor of (S)-4-[cis-2,6-dimethyl-4-(4-trifluoromethoxy-phenyl)-piperazine-1-sulfonyl]-indan-2-carboxylic acid tosylate (hereinafter optionally referred to as “Compound 1 tosylate”) was used for this experiment instead of Compound 1 tosylate due to the unsuitability of the Compound 1 tosylate crystals for X-ray structure determination. Compound 1 tosylate methyl ester was prepared via an esterification of Compound 1 tosylate followed by recrystallization from isopropanol. Other experiments have established that the stereochemistry is retained in converting the methyl ester to Compound 1 tosylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863276B2
Source datasetuspto-grants-2011_01
ORD IDord-a67dd3abc5b34ca3b4a0be879f6a7f7a
Source noteuspto-grants-2011_01