Methanol → Methyl L-threoninate hydrochloride

Thionyl chloride (39.0 ml, 0.542 mole) was added dropwise with stirring to 150 ml of dry methanol at -10° C. Then, 17.85 g. (0.15 mole) of D(+) threonine was added, cooling was discontinued and the reaction mixture was kept at about 22° C. for sixteen hours. The mixture was evaporated in vacuo to remove the solvent plus excess thionyl chloride, leaving crude D(+) threonine methyl ester HCl in essentially quantitative yield. The ester was dissolved in 375 ml saturated aqueous sodium bicarbonate, and the solution was stirred vigorously at about 22° C. while benzyl chloroformate (25.0 ml, 0.18 mole) was added dropwise over 5 minutes. The product separated as an oil which spontaneously crystallized after about 16 hours. This product was extracted into ether and after drying over anhydrous magnesium sulfate and evaporation, 42.8 g of white solid was obtained. Recrystallization from ethyl acetate/hexane gave two crops of product: (a) 30.91 g, m.p. 89.5°-91.5° C. and (b) 3.43 g, m.p. 87°-89° C.; total yield was 71%. Analysis calculated for C13H17NO5 : C=58.42%; H=6.41%; N=5.24%. Found: C=58.50%; H=6.45%; N=5.21%.

1. temperaturecooling
2. waitthe reaction mixture was kept at about 22° C. for sixteen hours
3. customThe mixture was evaporated in vacuo
4. customto remove the solvent plus excess thionyl chloride

ORD record

ord-4aaf1f1cba37461185f9e501e5d6e045

Source dataset

uspto-grants-1983_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04423029