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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 24571Erstellt: 23. Oktober 2026

Thiophenol → 4,4-Dimethyl-7-bromo-1-phenylthio-3,4-dihydronaphthalene

https://huagongshe.com/de/reaction/24571

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThiophenolHCID 7969—
EduktTetrahydrofuranHCID 8028—
EduktTriethylamineHCID 8471—
Edukt7-Bromo-4,4-dimethyl-1,2,3,4-tetrahydronaphthalen-1-oneHCID 10753357—
KatalysatorTitanium TetrachlorideHCID 24193—
LösungsmittelWaterHCID 962—
Produkt4,4-Dimethyl-7-bromo-1-phenylthio-3,4-dihydronaphthaleneHCID 15896018—

Reaktionsschritte

To a stirred solution of 4,4-dimethyl-7-bromo-3,4-dihydronaphthalen-1(2H)one (Compound G, 1.48 g, 5.9 mmol), titanium tetrachloride (1.09 g, 5.7 mmol) and THF (10 mL) was added a mixture of thiophenol (660 mg, 6 mmol), triethylamine (1.16 g, 11.5 mmol) and THF (20 mL) via an addition funnel at ambient temperature. The mixture was stirred for 5 h, and water (10 mL) was added, extracted with ether (3×50 mL). The combined organic layer was washed successively with water (10 mL), 10% NaHCO3 (10 mL) and brine (10 mL). The organic layer was dried (MgSO4) and the solvent distilled off at reduced pressure. After silicagel chromatography the title compound was obtained as a colorless oil

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06855832B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-60e46af075ba419ea97873f93ff81cab
Quellennotizuspto-grants-2005_02