Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772403Generated: November 2, 2026

p-Toluenesulfonic acid monohydrate → 7-(3,5-Di-tert-butylphenyl)-2-((1-methylcyclohexyl)methyl)-1H-indene

https://huagongshe.com/reaction/1772403

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 117817929HCID 117817929—
SolventTolueneHCID 1140—
Product7-(3,5-Di-tert-butylphenyl)-2-((1-methylcyclohexyl)methyl)-1H-indeneHCID 12346084781%

Reaction Steps

A mixture of p-toluenesulfonic acid monohydrate (0.88 g, 4.64 mmol, 0.2 equiv), compound 14 (10.0 g crude, 23.22 mmol, 1.0 equiv) and toluene (200 mL) was refluxed for 1 h. After cooling to room temperature, the mixture was washed sequentially with saturated sodium bicarbonate (100 mL) and saturated brine (100 mL). The organic layer dried over sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified on an AnaLogix (65-200 g) column, eluting with heptanes to give compound 15 (7.8 g, 81% yield for 2 steps) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249239B2
Source datasetuspto-grants-2016_02
ORD IDord-2c49f5c181e144ecbf9ff433d6d14fa9
Source noteuspto-grants-2016_02