HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Butenamide, N-(4-fluorophenyl)-3-methyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Fluoroaniline | HCID 9731 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 3-Methyl-2-butenoic acid | HCID 10931 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Butenamide, N-(4-fluorophenyl)-3-methyl- | HCID 532091 | — |
Reaction Steps
A solution of 10.0 g (0.1 mol) of 3-methyl-2-butenoic acid in 200 ml of THF is mixed with 9.4 ml (0.1 mol) of ethyl chloroformate and 14.1 ml (0.1 mol) of triethylamine at 0° C. After 10 minutes at room temperature, 10.6 ml (0.11 mol) of 4-fluoroaniline is added to it. The batch is stirred for 1 hour at room temperature, diluted with water and extracted with ethyl acetate (1 l). The organic phase is washed with saturated NaCl, dried (Na2SO4) and concentrated by evaporation in a vacuum. The residue is purified by column chromatography on silica gel with hexane-ethyl acetate. Yield 18.8 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07166592B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-569ab97148bb46ae9d801ea3d11b03ce |
| Source note | uspto-grants-2007_01 |