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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1193025Erstellt: 26. Oktober 2026

Furfural → ([4-Bromo-2,6-dimethylphenyl]furan-2-yl)methanol

https://huagongshe.com/reaction/1193025

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFurfuralHCID 7362—
EduktAmmonium ChlorideHCID 25517—
Edukt5-Bromo-2-iodo-1,3-dimethylbenzeneHCID 2735573—
EduktHCID 178418918HCID 178418918—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt([4-Bromo-2,6-dimethylphenyl]furan-2-yl)methanolHCID 6670961182,5%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

4-Bromo-2,6-dimethyl-1-iodobenzene (5 g, 16 mmol) is dissolved in dry tetrahydrofuran (20 ml) and cooled to −78° C. under an atmosphere of dry nitrogen. Isopropylmagnesium chloride (2M solution in tetrahydrofuran, 10 ml, 20 mmol) is added dropwise with vigorous stirring over 30 minutes. When the addition is complete, the reaction is allowed to warm to room temperature and is stirred for 30 minutes at room temperature. The reaction mixture is cooled to −78° C. and a solution of 2-furaldehyde (2.4 g, 25 mmol) in dry tetrahydrofuran (10 ml) is added dropwise over 30 minutes. Once the addition is complete, the mixture is allowed to warm to room temperature and stirring continued for 2 hours. A solution of saturated aqueous ammonium chloride (30 ml). is added, and the mixture is extracted with dichloromethane (3×25 ml). The organic extracts are combined, washed with brine, dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give ([4-bromo-2,6-dimethylphenyl]furan-2-yl)methanol (3.71 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08680339B2
Quelldatensatzuspto-grants-2014_03
ORD IDord-0be7fb479df94a41b7e743df13130fc0
Quellennotizuspto-grants-2014_03