Reaktion #409110

ord-5e5143388a3a4ad29f602d445e8de9f5

Reaktionsgleichung

COc1cc(S(=O)(=O)Cl)cc(OC)c1OC
3,4,5-trimethoxybenzenesulfonyl chloride
COc1ccc(N)cc1O
3-hydroxy-4-methoxyaniline
COc1ccc(NS(=O)(=O)c2cc(OC)c(OC)c(OC)c2)cc1O
product
COc1ccc(NS(=O)(=O)c2cc(OC)c(OC)c(OC)c2)cc1O
1-[(3-Hydroxy-4-methoxyphenyl)aminosulfonyl]-3,4,5-trimethoxybenzene

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengenthe reaction mixture was concentrated
  2. 2
    Sonstigethe crude residue was purified by chromatography over silica

Vorschrift

To a solution of 3,4,5-trimethoxybenzenesulfonyl chloride (500 mg, 1.88 nmol) in methanol (10 mL) was added 3-hydroxy-4-methoxyaniline (523 mg, 3.76 mmol) at ambient temperature. After stirring for 1 h, the reaction mixture was concentrated and the crude residue was purified by chromatography over silica to afford 430 mg (62%) of product as fine white needles, m.p. 145-146° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06211167B1uspto-grants-2001_04