Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 68289249 | HCID 68289249 | — |
| Reactant | HCID 178418310 | HCID 178418310 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68289288 | HCID 68289288 | — |
Reaction Steps
After 0.15 g of 1-[2-fluoro-6-(8-fluoro-quinolin-3-yloxy)-phenyl]-ethanone was dissolved in 1.5 ml of tetrahydrofuran, and then the solution was cooled to −78° C., 0.3 ml of t-butylmagnesium chloride (2.0 M diethyl ether solution) was added dropwise. After the reaction temperature was increased to room temperature, the reaction solution was treated with dilute hydrochloric acid, and then the liquid was separated with ethyl acetate. The organic layer was concentrated and then purified by silica gel column chromatography to obtain 0.04 g of 2-[2-fluoro-6-(8-fluoro-quinolin-3-yloxy)-phenyl]-3,3-dimethylbutan-2-ol (Compound Number 30).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772200B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-7040ca28f40647258bb452fd7a1d853f |
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| Source note | uspto-grants-2014_07 |
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