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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 532863Erstellt: 24. Oktober 2026

Acetic Anhydride → 5-Iodo-1-methyl-3,4-dihydroisoquinoline

https://huagongshe.com/de/reaction/532863

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
Edukt2-(2-Iodophenyl)ethanamineHCID 10514616—
EduktN-(2-iodophenethyl)acetamideHCID 86711313—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt5-Iodo-1-methyl-3,4-dihydroisoquinolineHCID 86711315—

Reaktionsschritte

N-(2-iodophenethyl)acetamide. A solution of 2-(2-iodophenyl)ethanamine (13.5 g, 54.6 mmol) and Ac2O (10.3 mL, 109 mmol) in 1,4-dioxane (200 mL) was heated to 100° C. for 45 min. The reaction was then allowed to cool to RT and concentrated in vacuo. The resulting residue was taken up in DCM and washed with a saturated aq. solution of NaHCO3— gas formation! The organic phase was separated, dried over Na2SO4, filtered and concentrated in vacuo to give the title compound as a yellow oil (16.2 g) which was used as it is in the next step. UPLC-MS: MS 290.3 (M+H+); UPLC rt 0.96 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08853203B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-ed8a50e664244039ad822f31729a0b9c
Quellennotizuspto-grants-2014_10