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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 847596Erstellt: 25. Oktober 2026

Benzyl Chloride → Ethyl 2-benzyl-1,3-dithiane-2-carboxylate

https://huagongshe.com/reaction/847596

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl ChlorideHCID 7503—
EduktEthyl 1,3-dithiane-2-carboxylateHCID 88552—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 2-benzyl-1,3-dithiane-2-carboxylateHCID 30370988,5%

Reaktionsbedingungen

Temperatur-25 °C

Reaktionsschritte

A solution of 3.0 g (15.6 mmol) of 2-ethoxycarbonyl-1,3-dithiane in 40 ml of dry tetrahydrofuran was cooled under inert atmosphere to -78° C. and treated with 7.5 ml (15.6 mmol) of n-butyllithium. The resulting solution was warmed to -25° C., stirred for 20 min, recooled to -78° C., treated with 1.8 ml (15.6 mmol) of benzyl chloride, and stirred at ambient temperature for 16 h. After quenching with aqueous ammonium chloride, the mixture was extracted with ether, washed sequentially with water, aqueous sodium thiosulfate, and brine, dried over MgSO4, and concentrated in vacuo. Flash chromatography using 5% ethyl acetate in hexane gave 3.9 g (88%) of the desired compound. 1H NMR (CDCl3) δ 1.33 (t, J=7 Hz, 3H), 1.85 (qt, J=14, 3 Hz, 1H), 2.11 (dm, J=14 Hz, 1H), 2.69 (dt, J=14, 4 Hz, 2H), 3.23 (ddd, J=14, 12, 3 Hz, 2H), 3.38 (s, 2H), 4.27 (q, J=7 Hz, 2H), 7.25-7.35 (m, 5H). Mass spectrum (M+NH4)+ =300.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05142056
Quelldatensatzuspto-grants-1992_08
ORD IDord-66cd437431d34d62947087968164ac25
Quellennotizuspto-grants-1992_08