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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1362408Erstellt: 23. Oktober 2026

Water → 1-(benzofuran-5-yl)-N-methylmethanamine

https://huagongshe.com/de/reaction/1362408

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktMethylamineHCID 6329—
Edukt1-Benzofuran-5-carbaldehydeHCID 2773875—
EduktSodium borohydrideHCID 4311764—
LösungsmittelMethanolHCID 887—
Produkt1-(benzofuran-5-yl)-N-methylmethanamineHCID 2184361991%

Reaktionsschritte

Benzofuran-5-carbaldehyde (315 mg, 2.16 mmol) was dissolved in anhydrous methanol (10 mL). Methylamine (0.86 mL of 33% solution in ethanol, 6.91 mmol) was added and the reaction was stirred for 3 h. The solution was concentrated to a brown oil and then dissolved in anhydrous methanol (10 mL). Sodium borohydride (83.2 mg, 2.20 mmol) was added and the mixture was stirred overnight at room temperature. Water (5 mL) was added and the solution was concentrated. Sodium hydroxide (10 mL, 1N) was added and the aqueous layer was extracted with ethyl acetate (3×20 mL). Combined organic layers were dried over MgSO4, filtered and concentrated to afford benzofuran-5-yl-N-methylmethanamine (316 mg, 91%) as a light brown oil: 1H NMR (400 MHz, DMSO-d6) δ 7.93 (s, 1H), 7.56 (s, 1H), 7.50 (d, J=8.4 Hz, 1H), 7.25 (d, J=8.4 Hz, 1H), 6.90 (s, 1H), 3.70 (s, 2H), 3.17 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07879872B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-2c3692fce25041bbaecfb8fb992b4da6
Quellennotizuspto-grants-2011_02