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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745620Generated: October 26, 2026

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

https://huagongshe.com/reaction/745620

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-2-oxovaleric acidHCID 70—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantO-methyl-L-tyrosine N-MethylamideHCID 14303038—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 14303083HCID 1430308372.3%

Reaction Steps

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.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04599361
Source datasetuspto-grants-1986_07
ORD IDord-1f725cf520964bd6aca9cf2131cdfefd
Source noteuspto-grants-1986_07