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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308966Generated: October 25, 2026

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

https://huagongshe.com/reaction/2308966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantOxalic AcidHCID 971—
ReactantMethyl 2-(oxiran-2-ylmethoxy)benzoateHCID 279510—
ReactantN-(2-Aminoethyl)-4-methylbenzenesulfonamideHCID 301318—
SolventMethanolHCID 887—
ProductMethyl 2-[2-Hydroxy-3-[N-[2-[N-(4-methylphenylsulfonyl)amino]ethyl]amino]propoxy]benzoate OxalateHCID 13732868—

Reaction Steps

A solution of 2.15 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 recrystallized 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04692446
Source datasetuspto-grants-1987_09
ORD IDord-9a56a270cf6c40819de273747a148323
Source noteuspto-grants-1987_09