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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612895Generated: November 2, 2026

Hydrochloric Acid → HCID 15229448, compound

https://huagongshe.com/reaction/1612895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanethiolHCID 6343—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant3-[1-(4-Chlorobenzyl)-3-methyl-5-methoxyindol-2-yl]-2,2-dimethylpropanoic acidHCID 11740819—
SolventDichloromethaneHCID 6344—
ProductHCID 15229448HCID 15229448—

Reaction Steps

To a solution of 1.05 g (2.7 mmol) of 3-[1-(4-chlorobenzyl)-3-methyl-5-methoxyindol-2-yl]-2,2-dimethylpropanoic acid (EP 166,591, Example 22) and 800 μL of ethanethiol (10 mmol) in 20 mL of CH2Cl2 at -20° C. was added in portions 2.17 g (16 mmol) of AlCl3. The reaction turned light orange and was stirred at room temperature overnight. In the morning, the reaction was completed (tlc) and it was poured into a solution of 1N HCl and extracted 3× with CH2Cl2. The combined organic layers were washed with brine, dried (MgSO4), and filtered. The filtrate was evaporated and to the residual syrup (680 mg) was added 20 mL of Et2O followed by an ethereal solution of diazomethane. Evaporation of the solvent left the crude title compound which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05190968
Source datasetuspto-grants-1993_03
ORD IDord-6ecaff9f934c413db1ca2ebef8f17ca2
Source noteuspto-grants-1993_03