Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Reactant | HCID 21182744 | HCID 21182744 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21182612 | HCID 21182612 | 111.5% |
Reaction Steps
A 100 mL round bottom flask containing 300 mg (0.66 mmol) of 2-(4-methoxyphenyl)benzo[b]thiophen-3-yl 4-[3-(1-pyrrolidinyl)propyl]phenyl ketone (Part A) was filled with 20 g of pyridine hydrochloride. The flask was heated to 160° C. to melt the solid. After 16 h, the reaction was cooled to warm temperature, diluted with 50 mL of H2O, and transferred to separatory funnel containing 50 mL H2O and 50 mL of EtOAc. The two layers were separated and the aqueous layer was extracted with EtOAc (2×50 mL). The combined EtOAc layers were dried over Na2SO4 and concentrated in vacuo to give 325 mg of a yellow oil. Purification by radial chromatography (SiO2; gradient of 2-10% MeOH in CH2Cl2) afforded 200 mg (0.45 mmol; 69%) of the title compound as a viscous yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06265575B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-0b43bfb94eaf4dc6b59c272f7af0b190 |
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| Source note | uspto-grants-2001_07 |
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