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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2060936Erstellt: 26. Oktober 2026

2-Methyl-2-nitro-1,3-propanediol → 2-Methyl-2-nitro-1,3-propanediol-di-p-toluenesulfonate

https://huagongshe.com/reaction/2060936

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Methyl-2-nitro-1,3-propanediolHCID 6480—
Edukt4-Toluenesulfonyl chlorideHCID 7397—
EduktTriethylamineHCID 8471—
LösungsmittelDiethyl EtherHCID 3283—
Produkt2-Methyl-2-nitro-1,3-propanediol-di-p-toluenesulfonateHCID 5195535,7%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 2-methyl-2-nitro-1,3-propanediol (80 g, 0.592 mol) and triethylamine (131.8 g, 1.303 mol) in diethyl ether (250 ml) is added a solution of tosyl chloride (225.7 g, 1.184 mol) in diethyl ether (800 ml) between −15° and −20° C. The resulting suspension is stirred at 0° C. for 1 hour, then 18 hours at ambient temperature. The reaction mixture is filtered, the solid residue is taken up twice in ethyl acetate and stirred, the suspension being filtered again. The combined ethyl acetate layers are evaporated to dryness giving a first crop of crude product (175.8 g). The ether filtrate is washed with water (2×) and brine, dried (Na2SO4), filtered, and partly concentrated. The suspension is filtered giving another 15.0 g of product. The crude solid product (190.8 g, 73%) is used in the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08278464B2
Quelldatensatzuspto-grants-2012_10
ORD IDord-32974668cc244d5bbec78c16528d8615
Quellennotizuspto-grants-2012_10