HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 4-ethoxycarbonyl-(S,S)-2,4-dibenzylbutyryl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 4-ethoxycarbonyl(S,S)-2,4-dibenzylbutyric acid | HCID 14557731 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-ethoxycarbonyl-(S,S)-2,4-dibenzylbutyryl chloride | HCID 14997130 | — |
Reaction Steps
The starting material is prepared as follows: 4.0 g of (S,S)-2,4-dibenzylglutaric anhydride is refluxed in 40 ml of ethanol:toluene (3:2) overnight. The reaction mixture is concentrated to yield 4-ethoxycaronyl-(S,S)-2,4-dibenzylbutyric acid as an oil. Oxalyl chloride (3.5 ml) is added to the solution of 4.5 g of 4-ethoxycarbonyl(S,S)-2,4-dibenzylbutyric acid in 10 ml of methylene chloride. The mixture is stirred at room temperature overnight and evaporated to yield 4-ethoxycarbonyl-(S,S)-2,4-dibenzylbutyryl chloride, which is used as such without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05021430 |
| Source dataset | uspto-grants-1991_06 |
| ORD ID | ord-7a3ce01095a14097a9b2d71f6690a91a |
| Source note | uspto-grants-1991_06 |