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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15408Erstellt: 25. Oktober 2026

Iodine → Benzo[b]thiophen-7-yl-p-tolylmethanol

https://huagongshe.com/reaction/15408

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
Edukt4-MethylbenzaldehydeHCID 7725—
EduktAmmonium ChlorideHCID 25517—
EduktMagnesiumHCID 5462224—
Edukt7-Bromobenzo[b]thiopheneHCID 12045538—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBenzo[b]thiophen-7-yl-p-tolylmethanolHCID 6871778157%

Reaktionsschritte

A Grignard reagent was prepared using 7-bromobenzo-[b]thiophene (1.0 g), magnesium (0.13 g), a catalytic amount of iodine and tetrahydrofuran (3 mL) according to the general method. To the Grignard reagent solution was added a solution of 4-methylbenzaldehyde (0.62 g) in tetrahydrofuran (5 mL) at 0° C. under an argon atmosphere. The reaction mixture was stirred at room temperature overnight and a saturated ammonium chloride aqueous solution was added to the mixture. The mixture was extracted with diethyl ether, and the organic layer washed with brine and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on aminopropylated silica gel (eluent: tetrahydrofuran). Further purification by column chromatography on silica gel (eluent; n-hexane/ethyl acetate=6/1) gave the title compound (0.68 g) as yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732596B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-791f4186fc2a410a8b3514d9786fd950
Quellennotizuspto-grants-2010_06