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HRID 581656생성일: 2026년 10월 27일

Sodium Hydroxide → methyl 2-(N-tert-butylsulfamoyl)-4-hydrazinobenzoate

https://huagongshe.com/reaction/581656

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Stannous chloride dihydrateHCID 61436—
반응물Sodium BicarbonateHCID 516892—
반응물methyl 4-amino-2-(N-tert-butylsulfamoyl)benzoateHCID 10946074—
반응물Sodium NitriteHCID 23668193—
용매Hydrochloric AcidHCID 313—
용매WaterHCID 962—
생성물methyl 2-(N-tert-butylsulfamoyl)-4-hydrazinobenzoateHCID 2171618270%

반응 단계

25.0 g (0.087 mol) of methyl 4-amino-2-(N-tert-butylsulfamoyl)benzoate are suspended in a mixture of 150 ml of concentrated HCl and 130 ml of water. A solution of 7.8 g (0.114 mol) of sodium nitrite is added dropwise at 0-5° C. A small amount of undissolved constituents are filtered off cold and the still cold diazonium salt solution is allowed to run slowly at 0° C. into a suspension of 55.0 g (0.244 mol) of SnCl2.2H2O in 55 ml of concentrated HCl. The mixture is subsequently stirred for 30 minutes and is then left to stand for 15 hours, while cooling with ice. Most of the HCl is first neutralized by addition of 6 N NaOH and the pH is then brought to about 6 with solid NaHCO3. The mixture is extracted several times with ethyl acetate, the extracts are dried and the solvent is removed in vacuo. After trituration of the residue with diisopropyl ether and drying, 18.3 g (70% of theory) of methyl 2-(N-tert-butylsulfamoyl)-4-hydrazinobenzoate of melting point 133-136° C. are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05922645
출처 데이터셋uspto-grants-1999_07
ORD IDord-169d15d6fcd7419582442516665faff0
출처 메모uspto-grants-1999_07