HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → D-leucic acid 4-nitrobenzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Reactant | (R)-2-hydroxy-4-methylpentanoic acid | HCID 439960 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | D-leucic acid 4-nitrobenzyl ester | HCID 86744637 | 98% |
Reaction Steps
10.45 g of D-leucic acid was dissolved in 150 ml of ethyl acetate. 11 ml of triethylamine and 18.78 g of 4-nitrobenzyl bromide were added and the mixture was heated under reflux for 3 hours. The mixture was washed in sequence with water, 10% citric acid solution, saturated sodium hydrogen carbonate solution, water and saturated sodium chloride solution. After drying over anhydrous sodium sulfate and evaporation, there were obtained 20.6 g (98%) of D-leucic acid 4-nitrobenzyl ester as a gum. Rf (chloroform) 0.37.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04996358 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-09c4995c8d274c228b43eff3835e827b |
| Source note | uspto-grants-1991_02 |