HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1362366Erstellt: 25. Oktober 2026
Methylamine → (3-Chloro-benzofuran-2-ylmethyl)methylamine
https://huagongshe.com/reaction/1362366
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Methylamine | HCID 6329 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 3-Chlorobenzofuran-2-carboxaldehyde | HCID 4737020 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | (3-Chloro-benzofuran-2-ylmethyl)methylamine | HCID 59277587 | 82,1% |
Reaktionsschritte
To a solution of 3-chlorobenzofuran-2-carboxaldehyde (1.62 g, 8.9 mmol) in methanol (50 mL) is added N-methylamine (33% solution in ethanol, 1.11 g, 35.9 mmol) and stirred overnight at room temperature. The mixture is concentrated in vacuo, re-solvated in methanol (50 mL) and cooled in an ice bath. Sodium borohydride (407 mg, 10.8 mmol) is added in portions and the mixture stirred at room temperature for 4 h. The mixture is concentrated in vacuo, re-solvated in 1.3M sodium hydroxide solution, stirred for 20 min, extracted with ethyl acetate, dried with sodium sulfate and concentrated. Purification by column chromatography (silica, CH2Cl2/MeOH, 9/1) gave title compound (1.43 g, 82%) as a colorless oil. 1H NMR (300 MHz, DMSO-d6) δ 7.55-7.63 (m, 2H), 7.33-7.42 (m, 2H), 3.93 (s, 2H), 2.27 (s, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07879872B2 |
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| Quelldatensatz | uspto-grants-2011_02 |
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| ORD ID | ord-460640b88e1d4bb8977386d0a7e38603 |
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| Quellennotiz | uspto-grants-2011_02 |
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