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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 654916Erstellt: 25. Oktober 2026

Iodine → HCID 19885920, Verbindung

https://huagongshe.com/reaction/654916

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
Edukt1-BromooctadecaneHCID 8218—
EduktMagnesiumHCID 5462224—
Edukt5-(Trimethylsilyl)furan-3-carbaldehydeHCID 15663251—
EduktHCID 178442890HCID 178442890—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 19885920HCID 19885920—

Reaktionsschritte

To a stirred solution of octadecylmagnesium bromide (10.2 ml of a 0.34M solution in ethyl ether, 3.46 mmol, generated from 1-bromooctadecane and magnesium using iodine as an initiator) at 0° under argon, was added dropwise 5-trimethylsilyl-3-furaldehyde (0.265 g., 1.57 mmol) in 2 ml tetrahydrofuran. This solution was allowed to warm to room temperature, stirred for 30 minutes, and quenched with a 5% ammonium chloride solution. The resulting mixture was partitioned between ethyl ether and 5% sodium bicarbonate. The organic portion was washed with 10% sodium bisulfite, water, saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated to give a residue. This was taken up in ethyl ether and filtered. The ether portion was concentrated to give a waxy residue which was purified by flash chromatography (silica, 10% ethyl ether/petroleum ether) to give the desired alcohol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05134128
Quelldatensatzuspto-grants-1992_07
ORD IDord-d47716d1b7bf40a5b7827c0ea24393c5
Quellennotizuspto-grants-1992_07