HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → Ethyl 2-benzyl-3-benzoyloxybutyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Ethyl 2-benzyl-3-hydroxybutyrate | HCID 13299637 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-benzyl-3-benzoyloxybutyrate | HCID 69304822 | 85% |
Reaction Steps
A mixture of 0.04 mol of ethyl 2-benzyl-3-hydroxybutyrate, 0.045 mol of pyridine, 0.05 mol of benzoyl chloride and 40 ml of dried tetrahydrofuran (THF) was refluxed by heating for 8 hrs, and then was allowed to react at room temperature for further 12 hrs. Upon the completion of the reaction, the reaction mixture was filtered, and the solid component was wished with diethyl ether for three times. The organic phases were combined, wished well with saturated saline, and then dried over anhydrous sodium sulfate. After removing the solvent, residue was subjected to column chromatography to give a colorless liquid. Yield 85%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351778B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-3ccbfa23d63e451cbbc721eb9ff5efdf |
| Source note | uspto-grants-2008_04 |