HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594778Generated: October 31, 2026
p-Toluenesulfonic acid → HCID 176531325, compound
https://huagongshe.com/reaction/1594778
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1-Undecanol | HCID 8184 | — |
| Reactant | HCID 178513185 | HCID 178513185 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 176531325 | HCID 176531325 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06284798B1 |
|---|
| Source dataset | uspto-grants-2001_09 |
|---|
| ORD ID | ord-7dceb5c455bf42b08466820e3d79f5e4 |
|---|
| Source note | uspto-grants-2001_09 |
|---|