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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 893559Erstellt: 23. Oktober 2026

Water → Acetate

https://huagongshe.com/de/reaction/893559

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt4-Toluenesulfonyl chlorideHCID 7397—
Edukt3-Butene-1,2-diolHCID 10338—
LösungsmittelPyridineHCID 1049—
ProduktAcetateHCID 175—
Produktp-ToluenesulfonateHCID 85570—

Reaktionsschritte

The racemic acetate substrate was prepared by one of two methods. The diol route began with racemic 1,2-dihydroxy-3-butene which could be prepared by reacting EpB with water under neutral conditions or with acid catalysis. The diol was treated with p-toluenesulfonyl chloride (p-TsCl) in pyridine at 4° C. to afford the desired monotosylate contaminated with about 10% of the corresponding ditosylate. The monotosylate could be selectively crystallized to afford pure monotosylate in 61% yield. Hydroxytosylate was acetylated under normal conditions (Ac2O, Et3N, CH2Cl2) to provide the acetoxy-tosylate (the desired racemic acetate) in 93% yield. The diol route is illustrated as follows: ##STR3##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05126268
Quelldatensatzuspto-grants-1992_06
ORD IDord-43103bb205504cc5b58c81ebba3f1cb6
Quellennotizuspto-grants-1992_06