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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2267294Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/2267294

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, 6 H), 5.93 (s, 2 H), 7.19 (dd, J=8, 2 Hz, 1 H), 7.37 (d, J=5 Hz, 1 H), 7.55 (d, J=5 Hz, 1 H), 7.66 (d, J=2 Hz, 1 H), 7.94 (d, J=9 Hz, 1 H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07858785B2
Quelldatensatzuspto-grants-2010_12
ORD IDord-b66ac67e2823491395836063477b0fd0
Quellennotizuspto-grants-2010_12