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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1743120Erstellt: 27. Oktober 2026

4-Methylmorpholine → Tert-butyl N-[(3S)-1-bromo-5-methyl-2-oxohexan-3-YL]carbamate

https://huagongshe.com/reaction/1743120

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
EduktDiazomethaneHCID 9550—
EduktL-Leucine, N-((1,1-dimethylethoxy)carbonyl)-HCID 83170—
Edukt2-Chloroethyl formateHCID 246748—
EduktAcetic Acid Mixture with Hydrobromic AcidHCID 21893785—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktTert-butyl N-[(3S)-1-bromo-5-methyl-2-oxohexan-3-YL]carbamateHCID 11034179—

Reaktionsschritte

Under atmosphere of argon, to a solution of (2S)-2-(t-butoxycarbonylamino)-4-methylpentanoic acid (t-butoxycarbonyl-L-leucine) (37.4 g) in tetrahydrofuran (800 ml) was added N-methylmorpholine (33 ml) at −25° C. and the mixture was stirred for 10 minutes. To the mixture was added chloroethylformate (15.8 ml) and the mixture was stirred for 20 minutes. Thereto was added a solution of diazomethane in diethyl ether and the mixture was stirred for another 2 hours. Thereto was added a mixture of 47% hydrobromic acid-acetic acid (1:1) at 0° C. and the mixture was stirred for 15 minutes. To the reaction mixture was added water and was extracted with a mixture of ethyl acetate-hexane. The organic layer was washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride successively, dried over anhydrous sodium sulfate and was concentrated. The residue was washed with cooled hexane to give the title compound (27.4 g) having the following physical data.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07008938B2
Quelldatensatzuspto-grants-2006_03
ORD IDord-d08d6bc59e7b400e8a04896dcd138cfd
Quellennotizuspto-grants-2006_03