Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 117759684 | HCID 117759684 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 117759605 | HCID 117759605 | — |
Reaction Steps
To a solution of ethyl 3-cyclopropyl-3-(3-(((2′-fluoro-2-(hydroxy(1-methylcyclopentyl)methyl)-5′-methoxybiphenyl-4-yl)oxy)methyl)phenyl)propanoate (99 mg) in THF (3 mL) was added thionyl chloride (64 μL) and the mixture was stirred at 50° C. for 15 hr. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (95 mg) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382188B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-32b76397b7b640ccb8d07485605a8d3a |
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| Source note | uspto-grants-2016_07 |
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