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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77323Erstellt: 23. Oktober 2026

Tetramethyltin → N-Isoamyl-N-(6-methyl naphthalene-2-sulfonyl)-D-valine tert-butyl ester

https://huagongshe.com/de/reaction/77323

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetramethyltinHCID 11661—
EduktLithium ChlorideHCID 433294—
EduktN-isoamyl-N-(6-trifluoromethanesulfonyloxy naphthalene-2-sulfonyl)-D-valine tert-butyl esterHCID 86653275—
KatalysatorHCID 178479802HCID 178479802—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-Isoamyl-N-(6-methyl naphthalene-2-sulfonyl)-D-valine tert-butyl esterHCID 6715528450%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of N-isoamyl-N-(6-trifluoromethanesulfonyloxy naphthalene-2-sulfonyl)-D-valine tert-butyl ester (1.1 g, 1.89 mmol) in N,N-dimethylformamide (20 mL) is added lithium chloride (0.40 g, 9.5 mmol), tetramethyl tin (0.525 mL, 3.79 mmol), and bistriphenylphosphino palladium dichloride (0.066 g, 0.095 mmol). The reaction is heated to 80° C. for 16 h. The reaction is allowed to cool to ambient temperature and filtered through Celite. The filtrate is poured over water and extracted three times with dichloromethane. The combined organic extracts were washed with brine, dried over sodium sulfate, and concentrated in vacuo. The residue is purified by column chromatography (4% hexanes-ethyl acetate) to afford the title compound as a white solid (0.41 g, 50% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841291B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-457daebb59124a8c80dea501b501c76d
Quellennotizuspto-grants-2014_09