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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 507828Erstellt: 25. Oktober 2026

Ammonium Chloride → tert-Butyl (3(S)-{[2-(3-methoxypropoxy)benzoylamino]methyl}-4-methyl-1(S)-vinylpentyl)carbamate

https://huagongshe.com/reaction/507828

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktPotassium bis(trimethylsilyl)amideHCID 3251421—
Edukttert-Butyl (1(S)-formyl-3(S)-{[2-(3-methoxypropoxy)benzoylamino]methyl}-4-methylpentyl)carbamateHCID 86613452—
KatalysatorMethyltriphenyliphosphonium bromideHCID 74505—
LösungsmittelDiethyl EtherHCID 3283—
Produkttert-Butyl (3(S)-{[2-(3-methoxypropoxy)benzoylamino]methyl}-4-methyl-1(S)-vinylpentyl)carbamateHCID 86613451—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

The mixture of 2.38 g of potassium bis(trimethylsilyl)amide in 50 ml of diethyl ether is cooled to 0° C., admixed with 4.04 g of methyltriphenylphosphonium bromide and stirred over 30 minutes. The solution of 1.70 g of tert-butyl (1(S)-formyl-3(S)-{[2-(3-methoxypropoxy)-benzoylamino]methyl}4-methylpentyl)carbamate in 20 ml of diethyl ether is added dropwise. The reaction mixture is stirred at room temperature over 1 hour and subsequently poured onto 1M ammonium chloride solution and extracted with tert-butyl methyl ether (2×). The combined organic phases are washed with water and brine, dried over sodium sulphate and concentrated by evaporation. The title compound is obtained from the residue by means of flash chromatography (SiO2 60F) as a slightly yellowish oil. Rf=0.36 (1:1 EtOAc-heptane); Rt=5.05 (gradient I).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07786307B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-d578bfab9fb24186aa8d4264818369c0
Quellennotizuspto-grants-2010_08