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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 324633Erstellt: 24. Oktober 2026

2,3-Dihydrobenzofuran-5-carboxaldehyde → (2,3-Dihydro-1-benzofuran-5-yl)methanol

https://huagongshe.com/de/reaction/324633

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,3-Dihydrobenzofuran-5-carboxaldehydeHCID 735901—
EduktSodium borohydrideHCID 4311764—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt(2,3-Dihydro-1-benzofuran-5-yl)methanolHCID 277615891%

Reaktionsschritte

To a solution of 2,3-dihydrobenzofuran-5-carbaldehyde (30.0 g, 0.202 mol) in methanol (150 mL) was added sodium borohydride (3.83 g, 0.101 mol) under ice-cooling. The mixture was stirred for 15 minutes at ambient temperature and then diluted with water. The product was extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate and evaporated. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to afford the title compound (yield 27.6 g, 91%) as an oily product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06218429B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-0e7457b7cc7c4102b4b04e499fc06b48
Quellennotizuspto-grants-2001_04