HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → N-ethoxycarbonylmethyl-4-(2,2,3,3-tetrafluoropropoxy)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Ethyl chloroacetate | HCID 7751 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-(2,2,3,3-Tetrafluoropropoxy)aniline | HCID 18766325 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-ethoxycarbonylmethyl-4-(2,2,3,3-tetrafluoropropoxy)aniline | HCID 19065104 | 78.9% |
Reaction Steps
A mixture of 8.6 g of 4-(2,2,3,3-tetrafluoropropoxy)aniline, 4.8 g of ethyl chloroacetate, 4.8 g of sodium bicarbonate, 3.0 g of sodium iodide and 300 ml of acetone was refluxed for 21 hours. The solvent was distilled off under reduced pressure and 200 ml of ice water and 200 ml of dichloromethane were added to the residue to fractionate. The dichloromethane layer was washed with water, dried over anhydrous magnesium sulfate and distilled off under reduced pressure. The residue was purified by silica gel column chromatography (eluted with ethyl acetate:hexane [1:3 v/v]) to give 9.4 g of N-ethoxycarbonylmethyl-4-(2,2,3,3-tetrafluoropropoxy)aniline as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05792780 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-8ebfda9ff34640f3a80fea79f747d573 |
| Source note | uspto-grants-1998_08 |