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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1743260Erstellt: 25. Oktober 2026

Ammonium Chloride → HCID 90791180, Verbindung

https://huagongshe.com/reaction/1743260

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt15-Crown-5HCID 36336—
Edukttert-butyl (2R,3S)-6-oxo-2,3-diphenylmorpholine-4-carboxylateHCID 981230—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
Edukt2-Trimethylsilanylethyl 4-iodopiperidine-1-carboxylateHCID 22238408—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 90791180HCID 90791180—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

4 g of tert-butyl (5S,6R)-2-oxo-5,6-diphenylmorpholine-4-carboxylate were dissolved in 50 ml of THF. 9 ml of 15-crown-5 were added, and the mixture was cooled to −78° C. Then 6.8 ml of a 2 M solution of NaHMDS in THF were added dropwise. The mixture was stirred for 10 min and then 8 g of 2-trimethylsilanylethyl 4-iodopiperidine-1-carboxylate were added dropwise. The mixture was allowed to warm to 0° C. over the course of 6 h, and then the reaction was stopped by adding 200 ml of saturated ammonium chloride solution. The aqueous phase was extracted 3 times with 150 ml of ethyl acetate each time, and the combined organic phases were dried with MgSO4. The solvents were removed in vacuo, and the residue was chromatographed on silica gel.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07008957B2
Quelldatensatzuspto-grants-2006_03
ORD IDord-3e41b89821224680bb8e0715a9e0af01
Quellennotizuspto-grants-2006_03