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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728965Generated: November 1, 2026

Hydrochloric Acid → HCID 18365658, compound

https://huagongshe.com/reaction/1728965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
ReactantDiethyl EtherHCID 3283—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 178418573HCID 178418573—
ProductHCID 18365658HCID 18365658—

Reaction Steps

140 ml (420 mmol) of a 3 M ethereal methylmagnesium bromide solution were added to a solution of 22.4 g (140 mmol) of a3 in 500 ml of diethyl ether at room temperature under Ar protection in the course of 1 hour. The mixture was then stirred under reflux at room temperature for another 2 hours, and was stirred at room temperature for a further 15 hours. The mixture was poured onto ice acidified with HCl, and extracted with ether. After the extract had been dried over sodium sulfate, the solvent was stripped off. The yellow oil which remained (20.3 g) was taken up in 800 ml of analytical grade toluene, 2.2 g (11.5 mmol) of p-toluenesulfonic acid hydrate were added and the mixture was refluxed for 45 minutes. After cooling, the solution was washed several times with water, dried over sodium sulfate and evaporated. The residue was chromatographed on 620 g of silica gel 60.5.5 g (25%) of the indene a4 (yellowish oil) could be eluted with hexane/methylene chloride (20:1). Still unused starting material a3 could be recovered with hexane/ethyl acetate (9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05329033
Source datasetuspto-grants-1994_07
ORD IDord-e0abd6483b3a4a25a4fe8438428e0c66
Source noteuspto-grants-1994_07