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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1731760생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1731760

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Oxalic AcidHCID 971—
반응물Methyl 2-(oxiran-2-ylmethoxy)benzoateHCID 279510—
반응물N-(2-Aminoethyl)-4-methylbenzenesulfonamideHCID 301318—
용매MethanolHCID 887—
생성물Methyl 2-[2-Hydroxy-3-[N-[2-[N-(4-methylphenylsulfonyl)amino]ethyl]amino]propoxy]benzoate OxalateHCID 13732868—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04623652
출처 데이터셋uspto-grants-1986_11
ORD IDord-56f42d917c074e938e6e5f2d16399366
출처 메모uspto-grants-1986_11