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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20354Erstellt: 25. Oktober 2026

Oxiranemethanol, 4-methylbenzenesulfonate, (S)- → Toluene-4-sulfonic acid 2-(S)-hydroxy-5-methylhexyl ester

https://huagongshe.com/reaction/20354

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxiranemethanol, 4-methylbenzenesulfonate, (S)-HCID 153296—
EduktHCID 178418816HCID 178418816—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktToluene-4-sulfonic acid 2-(S)-hydroxy-5-methylhexyl esterHCID 8749826975,5%

Reaktionsbedingungen

Temperatur2.5 °C

Reaktionsschritte

Add dropwise over 5 minutes isobutylmagnesium bromide (4.4 mL, 8.8 mmol, 2 M in diethyl ether) to a solution of lithium tetrachlorocuprate (4.4 mL, 0.44 mmol, 0.1 M in tetrahydrofuran) cooled to −35-40° C. Dissolve (2S)-(+)-glycidyl tosylate (1.674 g, 7.73 mmol) in tetrahydrofuran (8 mL), cool to −40° C. and cannulate into the stirring Grignard reaction flask. Quench with saturated aqueous ammonium chloride (25 mL), pour supernate into saturated aqueous ammonium chloride (25 mL) and water and shake well. Wash with saturated aqueous sodium chloride, dry (magnesium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 10:90 to 25:75 ethyl acetate:hexanes) to give the desired compound (1.6711 g, 75%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745438B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-3e73c66220eb47a0913b0234fe1c8597
Quellennotizuspto-grants-2010_06