HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 68536693, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | 6-(4-Fluorophenyl)pyridin-3-OL | HCID 46312788 | — |
| Reactant | [6-(2-Fluoro-phenyl)-pyridin-3-yloxy]-acetic acid tert-butyl ester | HCID 68536675 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68536693 | HCID 68536693 | — |
Reaction Steps
119 mg (2.72 mmol) of sodium hydride (55% in mineral oil) were added to 430 mg (2.27 mmol) of 6-(4-fluoro-phenyl)-pyridin-3-ol (prepared analogously as described in Example 76(a) to (d)) in 10 ml of DMF, and the mixture was stirred at room temperature for 60 min. Then 532 mg (2.72 mmol) of bromoacetic acid tert-butyl ester were added, and the reaction mixture was stirred at room temperature for 3 h. After evaporation, water and ethyl acetate were added. The organic phase was separated, dried, and evaporated. Yield: 433 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08188291B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-fdd0f3aced614d0a8afb922b1ea14767 |
| Source note | uspto-grants-2012_05 |