反応 #1153159

反応方程式

hexamethylenetetramine

4-(5-trifluoromethyl-tetrazol-1-yl)-phenol

trifluoroacetic acid

hexamethylenetetramine

H2SO4

→

title compound

収率 66.4%

2-Hydroxy-5-(5-trifluoromethyl-tetrazol-1-yl)-benzaldehyde

収率 66.4%

溶媒

water

反応条件

後処理

1. 1
   その他To a 2 L nitrogen purged round bottom flask fitted with a condenser
2. 2
   温度The solution was heated
3. 3
   温度to reflux
4. 4
   温度refluxed for 4 h
5. 5
   温度the solution refluxed overnight
6. 6
   温度The reaction was cooled
7. 7
   ろ過The yellow suspension was filtered
8. 8
   洗浄the cake washed with water until the filtrate
9. 9
   workup.DISSOLUTIONThe cake was dissolved in methylene chloride
10. 10
    ろ過filtered through 300 g of Silica Gel 60 (70-230 mesh)
11. 11
    その他flushed with 6 L of methylene chloride
12. 12
    その他The solvent was removed in vacuo
13. 13
    その他the residue flushed with hexanes
14. 14
    ろ過filtered
15. 15
    その他The white crystalline product that was obtained
16. 16
    その他was dried

実験手順

To a 2 L nitrogen purged round bottom flask fitted with a condenser was charged 67.7 g (0.29 mol) of 4-(5-trifluoromethyl-tetrazol-1-yl)-phenol, 540 mL trifluoroacetic acid, and 86.3 g (0.62 mol, 2.1 eq) of hexamethylenetetramine. The solution was heated to reflux and refluxed for 4 h. An additional 10 g (0.07 mol, 0.24 equiv) of hexamethylenetetramine was added and the solution refluxed overnight. The reaction was cooled and poured slowly into 3 L of 1N H2SO4. The suspension was diluted with an additional 500 mL of water and aged at room temperature for 30 min and at 0° C. and for additional 30 min. The yellow suspension was filtered and the cake washed with water until the filtrate was neutral. The cake was dissolved in methylene chloride and filtered through 300 g of Silica Gel 60 (70-230 mesh) and flushed with 6 L of methylene chloride. The solvent was removed in vacuo and the residue flushed with hexanes. The resulting slurry was cooled to room temperature and filtered. The white crystalline product that was obtained was dried yielding 50.4 g (66.4% yield) of the title compound. An additional 6.9 g (9.1%, for a combined yield of 57.3 g, 75.5% yield) was obtained by extracting the aqueous filtrate with ether and chromatographing (Silica Gel 60, methylene chloride): 1H NMR (CDCI3) δ 7.23 (d, J=9 Hz, 1H), 7.62 (dd, J=9, 2 Hz, 1H), 7.73 (d, J=2.5 Hz, 1H), 9.96 (s, 1H). MS (EI) m/z 258. Anal. Calcd for C9H5F3N4O2: C, 41.87; H, 1.95; F, 22.08; N, 21.70. Found: C, 41.87; H, 1.98; F, 22.61; N, 21.74.

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