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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 337639Erstellt: 24. Oktober 2026

N,N,N',N'-Tetramethylethylenediamine → 2-bromo-N-cyclopropyl-3,5-bis(3-methoxypropyl)benzamide

https://huagongshe.com/de/reaction/337639

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N,N',N'-TetramethylethylenediamineHCID 8037—
Edukt1,2-Dibromo-1,1,2,2-tetrafluoroethaneHCID 31301—
EduktN-cyclopropyl-3,5-bis(3-methoxypropyl)benzamideHCID 57456873—
EduktHCID 178418306HCID 178418306—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-bromo-N-cyclopropyl-3,5-bis(3-methoxypropyl)benzamideHCID 66896622—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a THF (0.1 M) solution of N-cyclopropyl-3,5-bis(3-methoxypropyl)benzamide (1 eq.) from the previous step and freshly distilled TMEDA (1 eq.) was added at −78° C. t-butyl lithium (1.7 M in pentanes, 1 eq.) dropwise over 10 min. The resulting reaction mixture was then slowly warmed to 0° C. over 1 h and stirred at 0° C. for 1 h. With the now orange reaction solution re-cooled to −78° C., 1,2-dibromotetrafluoroethane was added neat, dropwise over 10 min. The cooling bath was removed and the reaction mixture was stirred at RT for 18 h. The reaction was then quenched with 1 N aq. NaOH and extracted with EtOAc. The combined organic extracts were washed further with 10% aq. HCl, water and brine, dried over Na2SO4, filtered, and the filtrate concentrated in vacuo. Purification of the crude product thus obtained by way of flash chromatography (SiO2, 9:1 (v/v) Hex:EtOAc→EtOAc) afforded the title compound as a pale yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889714B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-9202ab05e81c4cef8c0512b14eb53a01
Quellennotizuspto-grants-2014_11