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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 745620Erstellt: 26. Oktober 2026

4-Methyl-2-oxovaleric acid → HCID 14303083, Verbindung

https://huagongshe.com/reaction/745620

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Methyl-2-oxovaleric acidHCID 70—
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
EduktO-methyl-L-tyrosine N-MethylamideHCID 14303038—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 14303083HCID 1430308372,3%

Reaktionsschritte

4-Methyl-2-oxopentanoic acid (31.3 g., 0.24 mol.) was dissolved in dry dichloromethane (50 mls.) and the resultant solution was cooled to 0° C. To the solution was added dropwise oxalyl chloride (23.2 mls., 0.265 mol.), followed by dimethylformamide (0.5 ml.). The resultant mixture was stirred at 0° C. for 1 hour, and then heated under reflux for 5 minutes and then allowed to cool. O-Methyl-L-tyrosine N-Methylamide (50.0 g., 0.24 mol.) and triethylamine (37.1 mls., 0.265 mol.) were dissolved in dichloromethane (120 mls.) and the resultant solution added dropwise to the cooled reaction mixture. The mixture was allowed to warm to room temperature and stirred overnight. The mixture was poured into water (50 mls.) and the organic layer was removed. The aqueous layer was extracted with dichloromethane (30 mls.), the combined extracts were dried over anhydrous sodium sulfate and the solvent removed by evaporation in vacuo to yield a crude product as a yellow solid (85.1 g.). The crude product was recrystallized from tertiary butyl ethyl ether to yield N-(4-methyl-2-oxopentanoyl)-O-methyl-L-tyrosine N-methylamide (55.6 g.)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04599361
Quelldatensatzuspto-grants-1986_07
ORD IDord-1f725cf520964bd6aca9cf2131cdfefd
Quellennotizuspto-grants-1986_07