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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561440Generated: October 31, 2026

P-Chloroacetophenone → HCID 58392426, compound

https://huagongshe.com/reaction/561440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-ChloroacetophenoneHCID 7467—
ReactantEthyl 3-(4-chlorophenyl)-3-hydroxybutanoateHCID 89439—
Reactantindium(III)chlorideHCID 159675—
Reactant7-[(Methylsulfanyl)methyl]-1H-indoleHCID 58392187—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 58392426HCID 58392426—

Reaction Conditions

Temperature80 °C

Reaction Steps

3.42 g (14.10 mmol) of ethyl 3-(4-chlorophenyl)-3-hydroxybutanoate (preparation in analogy to the synthesis of Example 88A starting from 4-chloroacetophenone and ethyl acetate) and 3.12 g (14.10 mmol) of indium(III) chloride were added to 2.50 g (14.10 mmol) of the compound from Example 8A in 100 ml of toluene. The reaction mixture was stirred at 80° C. for 5 h. After cooling to RT, the reaction solution was mixed with water and ethyl acetate, and the solid was filtered off. The phases of the filtrate were separated, and the aqueous phase was extracted with ethyl acetate. The combined organic phases were dried over sodium sulfate, filtered and concentrated. Purification of the crude product by flash chromatography on silica gel (mobile phase: dichloromethane/methanol 95/5) and then by preparative HPLC (mobile phase: acetonitrile/water gradient) resulted in 0.98 g (17% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063234B2
Source datasetuspto-grants-2011_11
ORD IDord-569ec1b127a54c8e93bf6d49f3f68afb
Source noteuspto-grants-2011_11