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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 507519Erstellt: 27. Oktober 2026

Acetic Acid → (benzo[b]thiophen-5-yl)-2,5-dimethyl-1H-pyrrole

https://huagongshe.com/reaction/507519

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt2,5-HexanedioneHCID 8035—
EduktBenzo(b)thiophen-5-amineHCID 288032—
LösungsmittelBenzeneHCID 241—
LösungsmittelDiethyl EtherHCID 3283—
Produkt(benzo[b]thiophen-5-yl)-2,5-dimethyl-1H-pyrroleHCID 5742882097%

Reaktionsschritte

A stirred solution of benzo[b]thiophen-5-amine (2.48 g, 17.0 mmol), hexane-2,5-dione (1.95 mL, 17.0 mmol) and glacial acetic acid (0.2 mL) in benzene (35 mL) was heated to reflux under a Dean-Stark head. After 14 h the reaction was cooled to r.t., diluted with diethyl ether (40 mL), and successively washed with aqueous 2 N hydrochloric acid (30 mL), brine (30 mL), a saturated aqueous solution of sodium hydrogen carbonate (30 mL) and finally brine (30 mL). The organic layer was separated, dried over magnesium sulfate, filtered and the solvent evaporated in vacuo to yield 1-(benzo[b]thiophen-5-yl)-2,5-dimethyl-1H-pyrrole (3.67 g, 97%) as a light orange crystalline solid. 1H NMR δ (CDCl3, 400 MHz) 2.04 (s, 6H), 5.93 (s, 2H), 7.19 (dd, J=8, 2 Hz, 1H), 7.37 (d, J=5 Hz, 1H), 7.55 (d, J=5 Hz, 1H), 7.66 (d, J=2 Hz, 1H), 7.94 (d, J=9 Hz, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07786132B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-8342a0c1c88440498e843b86ded8c66b
Quellennotizuspto-grants-2010_08