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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1724658Erstellt: 26. Oktober 2026

Isobutyraldehyde → Methyl 2-(isobutylamino)thiophene-3-carboxylate

https://huagongshe.com/reaction/1724658

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsobutyraldehydeHCID 6561—
EduktMethyl 2-amino-3-thenoateHCID 78381—
EduktSodium triacetoxyborohydrideHCID 5049666—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 2-(isobutylamino)thiophene-3-carboxylateHCID 67317044—

Reaktionsschritte

To a solution of methyl 2-aminothiophene-3-carboxylate (2.0 g, 12.7 mmol) in dichloromethane (40 mL) and glacial acetic acid (0.72 mL) were added isobutyraldehyde (0.87 g, 12.1 mmol) and sodium triacetoxyborohydride (4.0 g, 18.9 mmol). The reaction mixture was stirred for 18 h at room temperature and concentrated. The residue was dissolved in ethyl acetate, washed with aqueous sodium bicarbonate solution and with water, dried over anhydrous sodium sulfate and concentrated. The residual oil was purified on a silica gel flash chromatography column eluted with 5% ethyl acetate-hexane to afford the title compound as a slightly yellow oil (2.19 g, 81% yield). 1H NMR (400 MHz, CDCl3): δ 7.00 (d, 1 H), 6.18 (d, 1 H), 3.80 (s, 3 H), 3.20 (m, 2 H), 1.68 (m, 1 H), 1.00 (d, 6 H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07488736B2
Quelldatensatzuspto-grants-2009_02
ORD IDord-eb82c9ce6d23483caa90f652c375968f
Quellennotizuspto-grants-2009_02