Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

2,4-di-tert-butyl-6-[(E)-(hydroxyimino)methyl]phenol synthesis

2synthesis methods
37942-07-7 Synthesis
3,5-Di-tert-butylsalicylaldehyde

37942-07-7
372 suppliers
$5.00/5g

2,4-di-tert-butyl-6-[(E)-(hydroxyimino)methyl]phenol

118371-00-9
5 suppliers
inquiry

-

Yield:118371-00-9 98%

Reaction Conditions:

with pyridine;hydroxylamine hydrochloride in ethanol at 80; for 2 h;

Steps:

1B.B1

[00296] Section IB. 5-Aryl Phenol Oxadiazole Ligands Scheme Bl; [00297] A reaction flask was charged with BB7 (1.0 g, 4.23 mmol), hydroxylamine hydrochloride (356 mg, 5.12 mmol), EtOH (8.0 mL), and pyridine (0.41 mL, 5.12 mmol). The reaction was heated at 8O°C for 2h. Ethanol was removed by rotary evaporation and the reaction mixture was taken up in Et2O / H2O. The layers were separated and the organic layer was washed with H2O, brine, and then dried over Na2SO4. Isolated 1.04 g, 98% yield, of 3,5-di-t-butyl-2-hydroxybenzaldehyde oxime as a white solid. 1H NMR (300 MHz, C6D6) δ 1.23 (s, 9H, 'Bu), 1.64 (s, 9H, tBu), 6.06 (s, 1H, NOH), 6.72 (d, 1H), 7.50 (d, 1H), 7.84 (s, 1H), 10.49 (s, 1H, OH). EPO

References:

WO2006/66126,2006,A2 Location in patent:Page/Page column 71