Ethanolamine → 2-(Aminomethyl)phenol
Reaction equation
C([C:5]1[CH:10]=[CH:9][C:8]([OH:11])=[CH:7][CH:6]=1)(C)(C)C.C([CH2:14][NH2:15])O.C=O.P(=O)(O)(O)O>C(O)C.O>[OH:11][C:8]1[CH:7]=[CH:6][CH:5]=[CH:10][C:9]=1[CH2:14][NH2:15]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
An o-hydroxybenzylamine compound of the present invention composition was prepared according to the procedure of Example 1, except that 50 g of 4-t-butylphenol was employed in place of the Bisphenol-A, 20.1 g of ethanolamine was employed in place of the 2-(methylamino)ethanol, and that heating of the reactants was only begun after the formaldehyde addition was completed. A 0.5 g sample of the product was dissolved in 500 ml of ethanol/water (1:4 by volume) and the pH of the solution was adjusted to 3.0 with phosphoric acid.
Workup
- temperaturethat heating of the reactants
Sources & evidence
- ORD record
- ord-7486f9fc336349f2b2dc1e0a870090b4
- Source dataset
- uspto-grants-1988_12
- Patent number
- US04792355
Reaction notes
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