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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 916531Erstellt: 26. Oktober 2026

Triethylamine → HCID 58596253, Verbindung

https://huagongshe.com/reaction/916531

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktSodium HydroxideHCID 14798—
EduktTrifluoromethanesulfonic acidHCID 62406—
EduktBisulfiteHCID 104748—
Edukt2,3,4-TrifluorophenolHCID 123174—
EduktN,N-Diethylethanamine trihydrofluorideHCID 175505—
Edukt2-(6-{4-n-Propylcyclohexyl}spiro[3.3]hept-2-ylidene)[1,3]dithianeHCID 58596254—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 58596253HCID 58596253—

Reaktionsschritte

10.0 g (29.7 mmol) of the dithioacetal 6 are dissolved in 100 ml of dichloro-methane, and 2.6 ml (30.0 mmol) of trifluoromethanesulfonic acid are added dropwise with ice/common salt cooling. After 5 minutes, the cooling is removed, and the batch is stirred at room temperature for 45 minutes. The batch is subsequently cooled to −70° C., a mixture of 7.5 ml (54.0 mmol) of triethylamine and 6.67 g (45.0 mmol) of trifluorophenol in 30 ml of dichloromethane is added, and the mixture is stirred at −70° C. for 1 hour. 24.2 ml (0.150 mol) of triethylamine tris(hydrofluoride) are then added, and, after 5 minutes, 42.9 g (0.150 mol) of DBH, suspended in 60 ml of dichloromethane, are added in portions over the course of about 30 minutes. After 90 minutes, the batch is allowed to thaw and is hydro-lysed using 1 M sodium hydroxide solution and aqueous hydrogen sulfite solution. The organic phase is separated off, washed with saturated sodium chloride solution and dried over sodium sulfate. The solvent is removed under reduced pressure, and the residue is filtered through silica gel with n-heptane, giving the spiro compound 7 as a colourless solid of melting point: 43° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07270856B2
Quelldatensatzuspto-grants-2007_09
ORD IDord-25a79e9603f9477286e0a964f64d4e1e
Quellennotizuspto-grants-2007_09