HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561440Generated: October 31, 2026
P-Chloroacetophenone → HCID 58392426, compound
https://huagongshe.com/reaction/561440
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Chloroacetophenone | HCID 7467 | — |
| Reactant | Ethyl 3-(4-chlorophenyl)-3-hydroxybutanoate | HCID 89439 | — |
| Reactant | indium(III)chloride | HCID 159675 | — |
| Reactant | 7-[(Methylsulfanyl)methyl]-1H-indole | HCID 58392187 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58392426 | HCID 58392426 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063234B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-569ec1b127a54c8e93bf6d49f3f68afb |
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| Source note | uspto-grants-2011_11 |
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