HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(3-fluoro-2-formyl-phenyl)-acetamide → N-[3-fluoro-2-(hydroxyl-o-tolyl-methyl)-phenyl]-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(3-fluoro-2-formyl-phenyl)-acetamide | HCID 23106215 | — |
| Reactant | HCID 178424303 | HCID 178424303 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[3-fluoro-2-(hydroxyl-o-tolyl-methyl)-phenyl]-acetamide | HCID 69489997 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
100 mg (0.83 mmol) N-(3-fluoro-2-formyl-phenyl)-acetamide are dissolved in 4 ml of tetrahydrofuran and cooled to −78° C. Then at this temperature 1.66 ml (3.3 mmol) of a 2 M solution of o-tolylmagnesium bromide in diethyl ether are added. This reaction mixture is thawed to ambient temperature overnight with stirring. Then the reaction mixture is stirred into 30 ml dist. water and extracted three times with 10 ml of ethyl acetate. The organic phase is dried with MgSO4, the solvent is eliminated in vacuo. The crude product is purified by column chromatography. The carrier material used is silica gel and the eluant used is a mixture of cyclohexane:ethyl acetate (80:20).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07241769B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-db1a1fd68485452d9be4959907fbf2e0 |
| Source note | uspto-grants-2007_07 |