HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 14997137, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl L-leucinate | HCID 6451313 | — |
| Reactant | 4-(Pivaloyloxymethoxycarbonyl)-2,4-(R*,R*)-dibenzylbutyryl chloride | HCID 14997136 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14997137 | HCID 14997137 | — |
Reaction Steps
4-(Pivaloyloxymethoxycarbonyl)-2,4-(R*,R*)-dibenzylbutyryl chloride (1.2 g) in 10 ml of methylene chloride is added slowly to a solution of 0.60 g of (L)-leucine benzyl ester and 0.30 ml of triethylamine in 20 ml of methylene chloride. The reaction is stirred overnight at room temperature. The solution is washed with 2N hydrochloric acid, then with saturated sodium bicarbonate, dried over magnesium sulfate, filtered and concentrated to give N-[4-pivaloyloxymethoxycarbonyl-(R*,R*)-2,4-dibenzylbutyryl]-L-leucine benzyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05166212 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-54f6f9eb15164604b8369d781d352782 |
| Source note | uspto-grants-1992_11 |