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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348901Generated: October 25, 2026

Lithium hydroxide, monohydrate → 5-([Butyl(methyl)amino]methyl)thiophene-2-carboxylic acid

https://huagongshe.com/reaction/348901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantMethyl 5-{[butyl(methyl)amino]methyl}thiophene-2-carboxylateHCID 21086213—
SolventDioxane methanol waterHCID 22592949—
Product5-([Butyl(methyl)amino]methyl)thiophene-2-carboxylic acidHCID 21085960—

Reaction Steps

To a solution of methyl 5-{[butyl(methyl)amino]methyl}thiophene-2-carboxylate (280 mg, 1.16 mmol) in 2:1:1 dioxane/methanol/water (8.0 mL) is added lithium hydroxide monohydrate (146 mg, 3.38 mmol) and the reaction mixture stirred at room temperature overnight. The reaction mixture is concentrated under reduced pressure and the solid residue partitioned between ethyl acetate and water The aqueous phase is acidified to pH 1 with 1 N hydrochloric acid and extracted several times with 3:1 chloroform/2-propanol. The combined organic phase is washed with water, and brine, dried (sodium sulfate), filtered, and concentrated under reduced pressure to provide the title compound in pure form. 1H NMR (300 MHz, CD3OD) δ 7.75 (d, J=4 Hz, 1H), 7.41 (d, J=4 Hz, 1H), 4.63 (s, 2H), 3.20–3.14 (m, 2H), 2.85 (s, 3H), 1.82–1.72 (m, 2H), 1.42 (tq, J=8, 7 Hz, 2H), 0.99 (t, J=7 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176242B2
Source datasetuspto-grants-2007_02
ORD IDord-6d81c73ba8b9472c99cfbf32a12f1b4a
Source noteuspto-grants-2007_02