HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2104087Erstellt: 24. Oktober 2026
Isobutyraldehyde → Methyl 2-(isobutylamino)thiophene-3-carboxylate
https://huagongshe.com/de/reaction/2104087
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Isobutyraldehyde | HCID 6561 | — |
| Edukt | Methyl 2-amino-3-thenoate | HCID 78381 | — |
| Edukt | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Methyl 2-(isobutylamino)thiophene-3-carboxylate | HCID 67317044 | — |
Reaktionsschritte
To a solution of methyl 2-aminothiophene-3-carboxylate (2.0 g, 12.7 mmol) in dichloromethane (40 mL) and glacial acetic acid (0.72 mL) were added isobutyraldehyde (0.87 g, 12.1 mmol) and sodium triacetoxyborohydride (4.0 g, 18.9 mmol). The reaction mixture was stirred for 18 h at room temperature and concentrated. The residue was dissolved in ethyl acetate, washed with aqueous sodium bicarbonate solution and with water, dried over anhydrous sodium sulfate and concentrated. The residual oil was purified on a silica gel flash chromatography column eluted with 5% ethyl acetate-hexane to afford the title compound as a slightly yellow oil (2.19 g, 81% yield). 1H NMR (400 MHz, CDCl3): δ 7.00 (d, 1H), 6.18 (d, 1H), 3.80 (s, 3H), 3.20 (m, 2H), 1.68 (m, 1H), 1.00 (d, 6H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07576211B2 |
|---|
| Quelldatensatz | uspto-grants-2009_08 |
|---|
| ORD ID | ord-96af65fb2f2048049e951c853852fb92 |
|---|
| Quellennotiz | uspto-grants-2009_08 |
|---|