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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1604233Erstellt: 25. Oktober 2026

Diethyl Ether → 2-(1,1-Dimethylethoxy)-N-ethyl-1-naphthalenecarboxamide

https://huagongshe.com/reaction/1604233

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktN,N,N',N'-TetramethylethylenediamineHCID 8037—
EduktCyclohexaneHCID 8078—
EduktMagnesium BromideHCID 82241—
EduktN-ethyl-1-naphthalenecarboxamideHCID 4088726—
Eduktt-Butylperoxy benzoateHCID 21744378—
EduktCID 53628100HCID 178418400—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(1,1-Dimethylethoxy)-N-ethyl-1-naphthalenecarboxamideHCID 1960231933%

Reaktionsschritte

A solution of 1.3M s-BuLi in cyclohexane (34 mL, 44 mmol) was added dropwise to a -78° C. cooled solution of N-ethyl-1-naphthalenecarboxamide (20 mmol) and TMEDA (6.0 mL, 40 mmol) in THF (100 mL). After 30 min, MgBr2.Et2O (15.5 g, 60 mmol) was added portion wise, and the reaction was briefly warmed to ambient temperature then was recooled to -78° C. After 1 h at -78° C., t-butylperoxy benzoate (4.3 g, 22 mmol) was added. The resulting reaction was warmed to -30° C. and worked up in the usual manner, then was purified by chromatography with 3:7 ethyl acetate/hexanes to afford 1.7 g of desired compound as a white solid, a 33% yield. m.p. 126-127° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05994270
Quelldatensatzuspto-grants-1999_11
ORD IDord-9c54fa92272446849c5eb0d3d0b99cd6
Quellennotizuspto-grants-1999_11