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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1606709Erstellt: 25. Oktober 2026

Iodine → 5-Fluoro-2-methyl-1-(p-methylthiobenzyl)-indene

https://huagongshe.com/reaction/1606709

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktBenzyl ChlorideHCID 7503—
Edukt1-(Chloromethyl)-4-(methylthio)benzeneHCID 70128—
Edukt5-Fluoro-2-methylindan-1-oneHCID 3016257—
EduktMagnesiumHCID 5462224—
LösungsmittelDiethyl EtherHCID 3283—
Produkt5-Fluoro-2-methyl-1-(p-methylthiobenzyl)-indeneHCID 21521888—

Reaktionsschritte

13.44 G. (0.56 mole) of magnesium turnings were placed in a dried flask under N2 with 125 ml. of ether and a crystal of iodine. 6 Ml. of 65 ml. solution of 24.2 g. (0.14 mole) of p-methylthiobenzyl chloride in ether was added. After 3 to 5 minutes of stirring, the iodine color disappeared and the reaction began. After aging for 5 minutes, the rest of the benzyl chloride was added dropwise over 45 minutes. It was rinsed in with 10 ml. of ether and the reaction aged for 2 hours with stirring. 21 G. (0.128 mole) of 5-fluoro-2-methyl-1-indanone dissolved in 50 ml. of ether was added dropwise over 30 minutes. After aging for 1 hour, the milky supernatent mixture was decanted from the magnesium into 100 ml. of acetic acid. The flask and residual magnesium were rinsed into the acid solution with 4 × 50 ml. of benzene. 200 Ml. of water were added, the layers were separated and the organic layer was washed with 5 × 200 ml. water. It was stripped to dryness after drying over Na2SO4. The crude reaction product is crystallized from hexane to give pure 5-fluoro-2-methyl-1-(p-methylthiobenzyl)-indene, melting point 58°-59°C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03953520
Quelldatensatzuspto-grants-1976_04
ORD IDord-88cac19d4cd8460c85c5ca5c12669220
Quellennotizuspto-grants-1976_04