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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Edukt | 1,2-Dibromo-1,1,2,2-tetrafluoroethane | HCID 31301 | — |
| Edukt | N-cyclopropyl-3,5-bis(3-methoxypropyl)benzamide | HCID 57456873 | — |
| Edukt | HCID 178418306 | HCID 178418306 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-bromo-N-cyclopropyl-3,5-bis(3-methoxypropyl)benzamide | HCID 66896622 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08889714B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-9202ab05e81c4cef8c0512b14eb53a01 |
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| Quellennotiz | uspto-grants-2014_11 |
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