Sodium Hydroxide → 4-[Amino(phenyl)methyl]phenol

HRID 1940435

Reaktionsgleichung

Reaktionsgleichung von HRID 1940435
[OH:1][C:2]1[CH:16]=[CH:15][C:5]([C:6](=[N:13]O)[C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[CH:4][CH:3]=1.C([O-])(=O)C.[NH4+].C([BH3-])#N.[Na+].C(=O)([O-])O.[Na+].[OH-].[Na+]>[Cl-].[Cl-].[Cl-].[Ti+3].C(OCC)(=O)C>[OH:1][C:2]1[CH:3]=[CH:4][C:5]([CH:6]([NH2:13])[C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[CH:15][CH:16]=1

Komponenten

8

Versuchsvorschrift

A procedure similar to that described in Preparation 12 was repeated, but using 86 ml of a methanolic solution containing 4.28 g of 4-hydroxybenzophenone oxime, 17.03 g of ammonium acetate, 3.79 g of sodium cyanoborohydride, and 40.1 ml of a 17-19% by volume aqueous solution of titanium trichloride, and using a dilute aqueous solution of sodium hydrogencarbonate instead of the aqueous solution of sodium hydroxide, and using ethyl acetate as the extracting solvent. The residue obtained was subjected to silica gel column chromatography and eluted with a 80% by volume solution of ethyl acetate in hexane, with ethyl acetate itself, and with a 3% by volume solution of methanol in ethyl acetate, to give 2.74 g of the title compound as crystals, melting at 113°-115° C. (after recrystallization from methylene chloride).

Aufarbeitung

  1. customA procedure similar to that described in Preparation 12
  2. customThe residue obtained
  3. washeluted with a 80% by volume solution of ethyl acetate in hexane, with ethyl acetate itself
  4. customwith a 3% by volume solution of methanol in ethyl acetate, to give
  5. custom2.74 g of the title compound as crystals, melting at 113°-115° C. (after recrystallization from methylene chloride)

Quellen und Nachweise

ORD-Eintrag
ord-604618200bf4480dbb6ffc8b22f93165
Quelldatensatz
uspto-grants-1997_12
Patentnummer
US05698720

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