HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 2-bromo-2,2-difluoro-N-(4-fluoro-2-hydroxyphenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl bromodifluoroacetate | HCID 69585 | — |
| Reactant | 2-Amino-5-fluorophenol | HCID 185763 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-bromo-2,2-difluoro-N-(4-fluoro-2-hydroxyphenyl)acetamide | HCID 66836143 | 105.6% |
Reaction Conditions
| Temperature | -15 °C |
|---|
Reaction Steps
To 2-amino-5-fluorophenol (14 g, 110 mmol) in dry Tetrahydrofuran at 0° C. was added sodium hydride (55 wt % in mineral oil; 4.81 g, 110 mmol). The resulting mixture was stirred for 15 minutes at −15° C. Subsequently ethyl 2-bromo-2,2-difluoroacetate (24.59 g, 121 mmol) was added dropwise and the resulting mixture was stirred at 0° C. for two hours. The reaction mixture was quenched with saturated aqueous NH4Cl solution and extracted with ethyl acetate. The combined extracts were washed with brine, dried with Na2SO4 and concentrated to yield 33 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09066519B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-01a04fafaef54f8eb4063fc8deb6bb72 |
| Source note | uspto-grants-2015_06 |