HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 231837Erstellt: 26. Oktober 2026
Sodium hydride → 1-(2-propynyl)-2-trifluoromethyl-(1H)-indole
https://huagongshe.com/reaction/231837
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 1-Propyne, 1-bromo- | HCID 137279 | — |
| Edukt | 2-(trifluoromethyl)-1H-indole | HCID 10932124 | — |
| Edukt | Monosodium phosphate | HCID 23672064 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-(2-propynyl)-2-trifluoromethyl-(1H)-indole | HCID 17882579 | — |
Reaktionsschritte
8.57 g of 2-trifluoromethyl-1H-indole described in J. Org. Chem. (1983) 48-3233 and 10 ml of tetrahydrofuran were mixed together under an inert atmosphere at +5° C. and after 15 minutes, 2.4 g of sodium hydride in oil were added. After 2 minutes, 4.5 ml of 2-bromo-propyne were introduced and the resulting mixture was stirred for 30 minutes at +5° C., then for one hour at 25° C. Another 4.5 ml of bromo-propyne were added and the mixture was stirred for 4 hours and then poured into an iced solution of monosodium phosphate and extracted with ethyl ether. The extracts were concentrated to dryness by distillation under reduced pressure and the residue was chromatographed over silica and eluted with a mixture of hexane and ethyl acetate (95/5) to obtain 8.88 g of 1-(2-propynyl)-2-trifluoromethyl-(1H)-indole melting at 59° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04849443 |
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| Quelldatensatz | uspto-grants-1989_07 |
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| ORD ID | ord-0d5157f6691f44bab370f6cb3a62591d |
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| Quellennotiz | uspto-grants-1989_07 |
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