HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 563922Erstellt: 25. Oktober 2026
Diisopropylethylamine → HCID 59819988, Verbindung
https://huagongshe.com/reaction/563922
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Edukt | 3-(4-(Trifluoromethyl)phenyl)propionic Acid | HCID 3588736 | — |
| Edukt | 2-(5-Methyl-2-thienyl)ethanamine | HCID 14788189 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 59819988 | HCID 59819988 | 84,5% |
Reaktionsschritte
To a solution of 3 g (13 mmol) 4-(trifluoromethyl)hydrocinnamic acid (commercially available) in 30 mL DMF under argon were added 4.7 g (14.37 mmol) TBTU and 11.2 mL (65.3 mmol) N-ethyldiisopropylamine. A solution of 1.85 g (13 mmol) 2-(5-methyl-thiophen-2-yl)-ethylamine in 5 mL DMF was added drop wise over a period of 2 minutes. The mixture was stirred at room temperature for 1 h. The solvent was removed in vacuo and the residue was dissolved in ethyl acetate. The solution was washed with water and with a sat. NaHCO3 solution, dried over Na2SO4, filtered and concentrated in vacuo. The solid was stirred in 30 mL ether, filtered and dried. The mother liquor was concentrated in vacuo and purified on silica eluting with a gradient formed from heptane and ethyl acetate. The product containing fractions were evaporated. 3.75 g (84%) of the title compound was yielded as white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08067598B2 |
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| Quelldatensatz | uspto-grants-2011_11 |
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| ORD ID | ord-e2fa1dcde77e410c937eb3ef57d0f3d2 |
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| Quellennotiz | uspto-grants-2011_11 |
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