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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15173Erstellt: 25. Oktober 2026

Bromine → 7-Bromo-2,3-dihydro-1-benzofuran-5-carbaldehyde

https://huagongshe.com/reaction/15173

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromineHCID 24408—
EduktSodium AcetateHCID 517045—
Edukt2,3-Dihydrobenzofuran-5-carboxaldehydeHCID 735901—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelSodium ThiosulfateHCID 24477—
Produkt7-Bromo-2,3-dihydro-1-benzofuran-5-carbaldehydeHCID 1852618291,3%

Reaktionsschritte

To a solution of 2,3-dihydro-1-benzofuran-5-carbaldehyde (1.0 g, 6.75 mmol) in glacial acetic acid (8 ml) was added sodium acetate (664 mg, 8.1 mmol) and bromine (0.7 ml, 13.5 mmol) at 10° C. slowly. The reaction was stirred for 2 h at room temperature. The reaction was diluted with a saturated aqueous solution of sodium thiosulfate (10 ml), washed with a saturated aqueous solution of sodium bicarbonate, and then extracted with ethyl acetate. Organics were combined, dried over sodium sulfate and dried in vacuo to give the desired compound (1.4 g, 91%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732460B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-ccbd064e0acc467fae69302d4fe79d5f
Quellennotizuspto-grants-2010_06