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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348915Generated: October 25, 2026

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

https://huagongshe.com/reaction/348915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantN-MethylfurfurylamineHCID 78492—
ReactantMethyl 3-(hydroxymethyl)-5-methylbenzoateHCID 21086184—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-{[(2-furylmethyl)(methyl)amino]methyl}-5-methylbenzoateHCID 21086145—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176242B2
Source datasetuspto-grants-2007_02
ORD IDord-71253c5c484b44be9bdbbe7e4a8c4731
Source noteuspto-grants-2007_02