HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 57986691, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | tert-Butyldimethylsilyl trifluoromethanesulphonate | HCID 123564 | — |
| Reactant | HCID 67113825 | HCID 67113825 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 2,6-Lutidine | HCID 7937 | — |
| Product | HCID 57986691 | HCID 57986691 | — |
Reaction Steps
To a solution of 0.70 g of 3-chloro-4-(4-hydroxypiperidino)benzoic acid in 15 ml of methylene chloride, 1.5 ml of 2,6-lutidine and 2.7 g of tert-butyldimethylsilyltriflate were added, and the mixture was stirred at room temperature for 2 weeks. To the reaction solution, EtOAc was added, and the organic layer was washed with water and brine and then dried over sodium sulfate. After the evaporation of the solvent, the obtained residue was purified by silica gel column chromatography (eluent:hexane-EtOAc=5:1˜4:1) to obtain 0.90 g of 4-(4-tert-butyldimethylsilyloxypiperidino)-3-chlorobenzoic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338429B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-b547f790dbed408f847f0644d91390c9 |
| Source note | uspto-grants-2012_12 |