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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1731760Erstellt: 26. Oktober 2026

Acetone → Methyl 2-[2-Hydroxy-3-[N-[2-[N-(4-methylphenylsulfonyl)amino]ethyl]amino]propoxy]benzoate Oxalate

https://huagongshe.com/reaction/1731760

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktOxalic AcidHCID 971—
EduktMethyl 2-(oxiran-2-ylmethoxy)benzoateHCID 279510—
EduktN-(2-Aminoethyl)-4-methylbenzenesulfonamideHCID 301318—
LösungsmittelMethanolHCID 887—
ProduktMethyl 2-[2-Hydroxy-3-[N-[2-[N-(4-methylphenylsulfonyl)amino]ethyl]amino]propoxy]benzoate OxalateHCID 13732868—

Reaktionsschritte

A solution of 2.15 g of N-(2-aminoethyl)-p-toluenesulfonamide (0.1 mole) and 2.08 g of methyl 2-(2,3-epoxypropoxy)benzoate (0.01 mole) in 100 ml of methanol was stored at 25° C. for 4 hours. The methanol was then removed under reduced pressure, leaving an oil (NMR indicated only mono-alkylated product). The oil was then dissolved in 50 ml of methanol and an equimolar quantity of oxalic acid was added to the solution. 50 Ml of acetone was added, and the product crystallized upon refrigeration. The product was recrystallization from acetone/methanol (1:1) to yield 1.4 g of product which had a melting point of 165°-166° C. The elemental analysis (CHN) and NMR spectrum were consistent with the assigned structure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04623652
Quelldatensatzuspto-grants-1986_11
ORD IDord-56f42d917c074e938e6e5f2d16399366
Quellennotizuspto-grants-1986_11