HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → diethyl 2-(2,6-difluorophenyl)malonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Bromo-2,6-difluorobenzene | HCID 123557 | — |
| Reactant | Propanedioic acid, monoethyl ester | HCID 3595298 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | diethyl 2-(2,6-difluorophenyl)malonate | HCID 2782019 | — |
Reaction Steps
Into a mixture of 8.00 g of sodium hydride (60% in oil) and 100 ml of 1,4-dioxane, 32.0 g of ethyl malonate were added dropwise at 60° C. , further 14.6 g of cuprous bromide and 19.3 g of 1-bromo-2,6-difluorobenzene were added subsequently, and then refluxed for 16 hours under heating. To the reaction mixture, conc. hydrochloric acid was added under ice-cooling, and then tert-butyl methyl ether and water were added. The separated organic layer was washed with dil. hydrochloric acid and water subsequently, dried over sodium sulfate and concentrated. The residue was distilled under reduced pressure to give 16.5 g of diethyl (2,6-difluorophenyl)malonate. b.p. 107–109° C. (0.14 mmHg)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07211545B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-ac2f3bdbb4f14c87a2c1e4b306737d82 |
| Source note | uspto-grants-2007_05 |