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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 249102Erstellt: 23. Oktober 2026

Sodium borohydride → (2-Iodoquinolin-3-yl)methanol

https://huagongshe.com/de/reaction/249102

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium borohydrideHCID 4311764—
Edukt2-Iodoquinoline-3-carbaldehydeHCID 10989700—
LösungsmittelMethanolHCID 887—
Produkt(2-Iodoquinolin-3-yl)methanolHCID 1352719684,4%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a stirred solution of 2-iodo-3-quinolinecarboxaldehyde (595 mg, 2.10 mmol) in 40 mL of CH3OH at 0° C. was added NaBH4 (86 mg, 2.31 mmol), and the mixture was stirred at 0° C. for 30 min. After concentrating the mixture to approximately one-half of its original volume, water (30 mL) was added and the mixture was allowed to stand at 5° C. overnight. The solids were filtered and the crude product (570) mg, 95%) was recrystallized from methanol to give 3-hydroxymethyl-2-iodoquinoline (505 mg, 84%) as colorless needles: mp 189°-190° C. 1H NMR (300 MHz, CDCl3) δ 8.19 (s, 1H), 7.99 (d, 1H, J=9 Hz), 7.87 (d, 1H, J=9 Hz), 7.68 (m, 1H), 7.58 (t, 1H, J=9 Hz), 5.45 (t, 1H, J=6 Hz), 4.66 (d, 2H, J=6 Hz); IR (nujol) 3350, 1580, 1320, 1125, 1060, 995, 755, 720, cm-1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05212317
Quelldatensatzuspto-grants-1993_05
ORD IDord-93cdcc2e02a1464e830d4dbdf7b8a98a
Quellennotizuspto-grants-1993_05