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 2.0 g (0.0114 mole) of trans-3-(2,2-difluoroethenyl)-2,2-dimethylcyclopropanecarboxylic acid and 0.08 g of N,N-dimethylformamide in 20 ml of dry diethyl ether was cooled to 0° C. A solution of 2.17 g (0.017 mole) of oxalyl chloride 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 stirred 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-dimethylcyclopropanecarbonyl chloride as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04552892 |
| Source dataset | uspto-grants-1985_11 |
| ORD ID | ord-09f67cdf5ced41c2a5e474db5dc71168 |
| Source note | uspto-grants-1985_11 |