HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → trans-3-(2,2-Difluoroethenyl)-2,2-dimethylcyclopropanecarbonylchloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | trans-3-(2,2-Difluoroethenyl)-2,2-dimethylcyclopropanecarboxylic acid | HCID 67736179 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | trans-3-(2,2-Difluoroethenyl)-2,2-dimethylcyclopropanecarbonylchloride | HCID 86740007 | — |
Reaction Steps
A stirred solution of trans-3-(2,2-difluoroethenyl)-2,2-dimethylcyclopropanecarboxylic acid (2.0 g; 0.0114 mole) and N,N-dimethylformamide (0.08 g) in 20 ml of dry diethyl ether was cooled to 0° C. A solution of oxalyl chloride (2.17 g; 0.017 mole) in 2 ml of dry diethyl ether was added to the reaction mixture during a 20 minute period. Upon complete addition the mixture was allowed to warm to room temperature and stir for two hours. The mixture was concentrated under reduced pressure to give a yellow oil. The oil was dissolved in 5 ml of dry diethyl ether and the solvent removed under reduced pressure to yield trans-3-(2,2-difluoroethenyl)-2,2-dimethylcyclopropanecarbonylchloride as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04507317 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-4ded09a2eda446c19f6a01db7f6929b9 |
| Source note | uspto-grants-1985_03 |