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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 14123Erstellt: 25. Oktober 2026

Triethylamine → Methyl 3-{[(2-furylmethyl)(methyl)amino]methyl}-5-methylbenzoate

https://huagongshe.com/reaction/14123

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
EduktN-MethylfurfurylamineHCID 78492—
EduktMethyl 3-(hydroxymethyl)-5-methylbenzoateHCID 21086184—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 3-{[(2-furylmethyl)(methyl)amino]methyl}-5-methylbenzoateHCID 21086145—

Reaktionsschritte

To an ice-cold, stirred solution of methyl 3-(hydroxymethyl)-5-methylbenzoate (200 mg, 1.1 mmol) in methylene chloride (2.2 mL) is added triethylamine (0.304 mL, 2.2 mmol) followed by methanesulfonyl chloride (0.116 mL, 1.5 mmol). The reaction mixture is stirred for 15 min and filtered. N-Methylfurfurylamine (367 mg, 3.3 mmol) is added to the filtrate and the reaction mixture is stirred at room temperature for 5 h. The reaction mixture is diluted with methylene chloride (10 mL), washed with 1 N hydrochloric acid, and saturated sodium bicarbonate, dried (magnesium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 50% ethyl acetate/hexanes) provided the title compound. 1H NMR (300 MHz, CDCl3) δ 7.76 (d, J=11 Hz, 2H), 3.79 (d, J=6 Hz, 2H), 6.32 (d, J=2 Hz, 1H), 6.21 (d, J=3 Hz, 1H), 3.90 (s, 3H), 3.59 (s, 3H), 3.53 (s, 2H), 2.39 (s, 3H), 2.23 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07727997B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-4068ae73086f4ec5b761ba9531fd380b
Quellennotizuspto-grants-2010_06