HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467983Generated: October 30, 2026
Cesium carbonate → (6-Trifluoromethyl-pyridin-2-yl)-acetic acid ethyl ester
https://huagongshe.com/reaction/467983
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | 2-Bromo-6-(trifluoromethyl)pyridine | HCID 2782902 | — |
| Reactant | 2,2-Diethylpropanedioate | HCID 6951563 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | (6-Trifluoromethyl-pyridin-2-yl)-acetic acid ethyl ester | HCID 58216744 | — |
Reaction Steps
A mixture of caesium carbonate (1.87 g, 5.75 mmol) and tri-t-butylphosphine (107 μL, 0.44 mmol) in dry 1,2 dimethoxyethane (10 mL) was treated with tris-(dibenzylideneacetone)di-palladium (81 mg, 0.09 mmol), 2-Bromo-6-(trifluoromethyl)pyridine (1 g, 4.42 mmol) and diethylmalonate (0.8 mL, 5.3 mmol) under nitrogen atmosphere. The mixture was heated to 150° C. for 30 min in a microwave oven. After cooling to 20° C. the mixture was treated with a saturated solution of ammonium chloride (120 mL) and extracted with ethyl ether (3×80 mL). The organic phase was dried and evaporated to give a crude oil that was purified by flash chromatography eluting with n-hexane/ethyl ether 6/1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08623901B2 |
|---|
| Source dataset | uspto-grants-2014_01 |
|---|
| ORD ID | ord-324094b410cd4a10b7af947ebfe95bd2 |
|---|
| Source note | uspto-grants-2014_01 |
|---|