HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → L-Leucine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Bromo-1,1-dimethoxyethane | HCID 81672 | — |
| Reactant | Leucine methyl ester hydrochloride | HCID 2723695 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | L-Leucine | HCID 6106 | — |
Reaction Steps
A solution containing L-leucine methyl ester hydrochloride (2.9 g, 16 mmol), 2-bromo-1,1-dimethoxy ethane (1.9 ml, 2.7 g, 16 mmol), NEt3 (6.7 ml, 48 mmol) and a catalytic amount of KI in DMF (190 ml) was stirred at 120° C. for 3 days. The reaction mixture was concentrated under reduced pressure, diluted with water and extracted with DCM. The organic layer was then washed with brine, dried over Na2SO4 and evaporated. The crude product was purified by column chromatography (silica gel, EtOAc/P.E. 1:1) to afford compound of formula (III), where R=Leu side chain, as a yellow oil (1.2 g, 32% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08445484B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-55567e661dcb4205aafe5ec8a22e8489 |
| Source note | uspto-grants-2013_05 |