HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-{[3-Cyano-4-(trifluoromethyl)phenyl]amino}-2-oxoethyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acetoxyacetyl chloride | HCID 26297 | — |
| Reactant | 5-Amino-2-(trifluoromethyl)benzonitrile | HCID 12104958 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-{[3-Cyano-4-(trifluoromethyl)phenyl]amino}-2-oxoethyl acetate | HCID 66654537 | 71.6% |
Reaction Steps
Triethylamine (1.09 g, 10.8 mmol) was added to a stirred solution of 5-amino-2-(trifluoromethyl)benzonitrile (Intermediate 37, 1.0 g, 5.37 mmol) in DCM (40 mL), at 0° C., and the mixture was stirred for 15 min. Chloro-2-oxoethyl acetate (1.10 g, 8.06 mmol) was added at 0° C. and the mixture was stirred for 4 h at room temperature. The reaction mixture was diluted with DCM and washed with ice water, and saturated brine solution. The organic layer was dried over anhydrous Na2SO4, and concentrated under reduced pressure to afford the crude compound. This was purified by column chromatography (100-200 mesh silica gel), eluting with 20%-40% EtOAc/pet.ether to give the title compound (1.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115132B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-a39cd9a1d76e4c3b9fcd57eb7ecc80ca |
| Source note | uspto-grants-2015_08 |