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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582683Generated: November 2, 2026

p-Toluenesulfonic acid → HCID 69907470, compound

https://huagongshe.com/reaction/1582683

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 22718777HCID 22718777—
SolventBenzeneHCID 241—
SolventSodium BicarbonateHCID 516892—
ProductHCID 69907470HCID 6990747042.9%

Reaction Steps

To a solution of ethyl 3-hydroxy-3-(4′-cycloheptylphenyl)-butanoate (2c, 28.75 g) in benzene (175 ml) was added p-toluenesulfonic acid and was refluxed for 1 h. The reaction mixture was diluted with NaHCO3 and benzene layer was separated out. The organic layer was washed with water, dried (Na2SO4) and concentrated. The crude product was purified by column chromatography on silica gel to give 11.6 g (42.9% yield) of ethyl 3-(4′-cycloheptylphenyl)-but-2-enoate (3c, formula 3, R=cycloheptyl) as viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06737438B2
Source datasetuspto-grants-2004_05
ORD IDord-19269e2e21b14ed28fbf30e5aa705ec9
Source noteuspto-grants-2004_05