HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cesium carbonate → 1-(4-Trifluoromethyl-benzyloxy)-naphthalene-2-carboxylic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Naphthalenecarboxylic acid, 1-hydroxy-, methyl ester | HCID 70358 | — |
| Reactant | 1-(Bromomethyl)-4-(trifluoromethyl)benzene | HCID 123062 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(4-Trifluoromethyl-benzyloxy)-naphthalene-2-carboxylic acid methyl ester | HCID 68845172 | 90% |
Reaction Steps
To 3.26 g caesium carbonate and 1.01 g methyl 1-hydroxy-2-naphthoate in 10 ml abs. DMF was added 1.21 g 1-bromomethyl-4-trifluoromethyl-benzene and the mixture was reacted for 3 h at room temperature. The reaction was partitioned between water and ethyl acetate and the aqueous layer was extracted with ethyl acetate twice. The combined organic phases were dried over magnesium sulphate and concentrated in vacuo. The resulting residue was purified by chromatography (silica, heptane) to yield 1.62 g of 1-(4-trifluoromethyl-benzyloxy)-naphthalene-2-carboxylic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552033B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-d8e640ee29b44a91b2b103197ead0018 |
| Source note | uspto-grants-2013_10 |