HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Isobutyric acid 2-[2-(4-chlorophenyl)-acetyl]-5-fluoro-phenyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyryl chloride | HCID 62325 | — |
| Reactant | 2-(4-Chlorophenyl)-1-(4-fluoro-2-hydroxy-phenyl)-ethanone | HCID 68702520 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Isobutyric acid 2-[2-(4-chlorophenyl)-acetyl]-5-fluoro-phenyl ester | HCID 68702502 | — |
Reaction Steps
To a solution of 2-(4-chlorophenyl)-1-(4-fluoro-2-hydroxy-phenyl)-ethanone (16.0 g, 60.6 mmol) in CH2Cl2 (300 ml) is added triethylamine (7.4 g, 72.7 mmol). A solution of isobutyryl chloride (7.1 g, 66.6 mmol) in CH2Cl2 (100 ml) is added slowly over 30 min. The reaction mixture is stirred at room temperature for 2 h. The organic phase is washed with 0.5 M HCl, water and brine and dried (MgSO4). The solvent is removed in vacuo, and the product is purified by flash chromatography on silica gel using iso-hexane:ethyl acetate (20:1 to 10:1) as the eluent to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07732435B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-e958c84830ae426ab502612169257fb6 |
| Source note | uspto-grants-2010_06 |