p-Toluenesulfonic acid → HCID 176531325, compound

HRID 1594778Notes

Reaction equation

HRID 1594778 reaction equation
[CH2:1](O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11].C(=O)(O)O.[NH2:17][NH:18][C:19]([NH2:21])=[NH:20].C1(C)C=CC(S(O)(=O)=O)=CC=1>O.C1(C)C=CC=CC=1>[CH:1](=[N:17][NH:18][C:19]([NH2:21])=[NH:20])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11]

Participants

6

Procedure

1 mol (170.3 g) of undecanol, 1.1 mol (150 g) of aminoguanidine hydrogen carbonate and 1 g of p-toluenesulphonic acid are mixed with 500 ml of toluene and refluxed with stirring. As soon as 2 mol of water have been separated using the water separator, the mixture is allowed to cool, concentrated by rotary evaporation and the dark red oil is taken up in 250 ml of petroleum ether 40/60°. The precipitate formed is suction filtered and washed again with petroleum ether. For recrystallisation the precipitate is dissolved in ethyl acetate and mixed with petroleum ether at boiling temperature (boiling range 40 to 60° C.) until beginning to turn cloudy. Fine crystals are obtained, m.p. 101° C. The structure and purity of the compound were confirmed by analytical and spectroscopic data.

Workup

  1. temperaturerefluxed
  2. temperatureto cool
  3. concentrationconcentrated by rotary evaporation
  4. custom60°
  5. customThe precipitate formed
  6. filtrationfiltered
  7. washwashed again with petroleum ether
  8. customFor recrystallisation the precipitate
  9. dissolutionis dissolved in ethyl acetate
  10. additionmixed with petroleum ether at boiling temperature (boiling range 40 to 60° C.)
  11. customFine crystals are obtained

Sources & evidence

ORD record
ord-7dceb5c455bf42b08466820e3d79f5e4
Source dataset
uspto-grants-2001_09
Patent number
US06284798B1

Reaction notes

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