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HRID 36504Erstellt: 23. Oktober 2026

Ethyl Acetate → N-[3,3,3-Trifluoro-2-(mercaptomethyl)-1-oxopropyl]-L-leucine

https://huagongshe.com/de/reaction/36504

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktPotassium bisulfateHCID 516920—
EduktN-[2-[(Acetylthio)methyl]-3,3,3-trifluoro-1-oxopropyl]-L-leucineHCID 54059189—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelHexaneHCID 8058—
LösungsmittelAmmonium HydroxideHCID 14923—
ProduktN-[3,3,3-Trifluoro-2-(mercaptomethyl)-1-oxopropyl]-L-leucineHCID 53740741—

Reaktionsschritte

A suspension of the product of Example 18 (2.3 g., 6.98 mmol.) in 4.45 mL of concentrated ammonium hydroxide and 10 mL of water was stirred at room temperature under argon for 8 minutes. The resulting clear solution was acidified with 5% potassium hydrogen sulfate solution to pH 2 and extracted with 100 mL of ethyl acetate followed by 3×75 mL of additional extractions. The combined ethyl acetate extract was washed with 100 mL of brine, dried (MgSO4) and evaporated to give 1.94 g. of an off-white solid. Flash chromatography on 200 g. of silica gel eluting with ethyl acetate: hexanes:acetic acid, 100:100:1 afforded 1.72 g. of the title isomer A product as a white crystalline solid, m.p. 143°-145° C., TLC Rf =0.38 (100:50:1 ethyl acetate:hexane:acetic acid), [α]D =-62.2° (c=1.00, methanol).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05414013
Quelldatensatzuspto-grants-1995_05
ORD IDord-e9201d502a384a31b3a894e1357eef75
Quellennotizuspto-grants-1995_05