HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-(3,5-Difluorophenyl)acetyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3,5-Difluorophenylacetic acid | HCID 145424 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(3,5-Difluorophenyl)acetyl chloride | HCID 2782723 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
3,5-Difluorophenylacetic acid (30 g, 0.174 mol) (Aldrich) was dissolved in dichloromethane and this solution was cooled to 0° C. DMF (0.5 mL, catalytic) was added followed by the dropwise addition of oxalyl chloride (18 mL, 0.20 mol) over a 5 minute period. The reaction was stirred for 3 h and then rotoevaporated at reduced pressure to a residue which was placed on a high vacuum pump for 1 h to afford 3,5-difluorophenylacetyl chloride as a thin yellow oil. Other acid chlorides can be prepared in a similar manner.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211235B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-349d0a55ff5c4dd5afd9eec06e5761cd |
| Source note | uspto-grants-2001_04 |