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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1534843Erstellt: 26. Oktober 2026

Methanol → methyl 4-Amino-3-methylsulfonylbenzoate

https://huagongshe.com/reaction/1534843

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktThionyl ChlorideHCID 24386—
Edukt4-Amino-3-methanesulfonylbenzoic acidHCID 19096074—
Produktmethyl 4-Amino-3-methylsulfonylbenzoateHCID 22041468—

Reaktionsschritte

Precursors of Example 28 starting from 4-chloro-3-methylsulfonylbenzoic acid via 4-N-hydrazino-3-methylsulfonylbenzoic acid (m.p. 243°-245° C.) and its hydrogenolytic N-N cleavage with Raney nickel catalyst in methanol/aq. NH3 under normal pressure at room temperature to give 4-amino-3-methylsulfonylbenzoic acid (m.p. 258°-262° C.) and subsequent reaction with thionyl chloride and methanol to give methyl 4-amino-3-methylsulfonylbenzoate (m.p. 146° C.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05091394
Quelldatensatzuspto-grants-1992_02
ORD IDord-fd06a696134f4f858add862390c664a6
Quellennotizuspto-grants-1992_02