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HRID 1646584Erstellt: 26. Oktober 2026

1,3-Dithiane → 2-(3-Fluorophenyl)methyl-1,3-dithiane

https://huagongshe.com/reaction/1646584

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3-DithianeHCID 10451—
Edukt3-Fluorobenzyl bromideHCID 68007—
EduktButyllithiumHCID 178418339—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
Produkt2-(3-Fluorophenyl)methyl-1,3-dithianeHCID 1979323666,7%

Reaktionsbedingungen

Temperatur-23 °C

Reaktionsschritte

1,3-Dithiane (12 g, 0.1 mol) was dissolved in 150 mL of anhydrous THF under a nitrogen atmosphere. The resultant solution was cooled to -78° C. and n-butyllithium (44 mL of a 2.5M solution of in hexane, 0.11 mol) was added. The reaction mixture was warmed to -23° C. and then stirred at -23° C. for 0.5 h. The reaction mixture was recooled to -78° C. and 25 g (0.135 mol) of 3-fluorobenzyl bromide was added over a 15 minute period. The reaction mixture was stirred for 3 h at ambient temperature and then diluted with methylene chloride, washed with aqueous ammonium chloride solution and brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was distilled to afford 15.2 g (66.7% yield) of the title compound, b.p. 135°-140° C. (0.5 mm Hg); MS DCI-NH3M/Z: 229 (M+H)+ ; 1H NMR (CDCl3) δ1.77-1.95 (1H, m), 2.05-2.18 (1H, m), 2.8-2.9 (4H, m), 3.02 (2H, d, J=7.5 Hz), 4.23 (1H, t, J=7.5 Hz), 6.9-7.1 (3H, m), 7.23-7.33 (1H, m).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05180733
Quelldatensatzuspto-grants-1993_01
ORD IDord-f202a4206cc34fae9f58796f2eb83806
Quellennotizuspto-grants-1993_01