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HRID 1197942Erstellt: 26. Oktober 2026

Chloride → tert-Butyl 2,4-dideoxy-3,5-O-(1-methylethylidene)-D-erythro-hexonate

https://huagongshe.com/reaction/1197942

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorideHCID 312—
EduktN-methyl-2-pyrrolidoneHCID 13387—
Eduktchloride (4R-cis)-6-(chloromethyl)-2,2-dimethyl-1,3-dioxane-4-acetic acid, 1,1-dimethylethyl esterHCID 86747487—
KatalysatorTetrabutylammonium AcetateHCID 82707—
Produkttert-Butyl 2,4-dideoxy-3,5-O-(1-methylethylidene)-D-erythro-hexonateHCID 9816650—

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

Solid tetrabutylammonium acetate obtained as above (111 g, 0.368 mole) was added in one portion to a mechanically stirred solution of the chloride (4R-cis)-6-(chloromethyl)-2,2-dimethyl-1,3-dioxane-4-acetic acid, 1,1-dimethylethyl ester prepared in step (d) above (35 g, 0.125 mole) in HPLC grade 1-methyl-2-pyrrolidinone (504 ml) under argon. The resulting solution was stirred at 85° C. (internal temperature). After 30 to 60 minutes the reaction mixture became homogeneous and brown in color. The progress of the reaction was followed by TLC and GC analysis. (TLC: Rf=0.63 for the chloride starting material; Rf =0.54 for the title compound (silica gel, Ethyl acetate:Hexane, 1:1, visualization by Ce(SO4)2 spray). GC: Rt =7.20 minutes (starting material) and 8.66 minutes (title compound).) After 11 hours the reaction was completed.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05278313
Quelldatensatzuspto-grants-1994_01
ORD IDord-02c9ee7d251a479997b30a754de1ef23
Quellennotizuspto-grants-1994_01