Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178479531 | HCID 178479531 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178479532 | HCID 178479532 | — |
Reaction Steps
The preparation of the subject compound may also be accomplished as follows: 25 g. of 1,3-diaminoguanidine hydrochloride is dissolved in 1800 ml. of boiling ethanol. To this boiling solution, 28 g. of 4-chlorobenzaldehyde in 300 ml. of ethanol is added over a period of 8 hours. The reaction mixture is then cooled at 0° C. overnight, clarified, and the filtrate concentrated to 500 ml. volume and cooled at 0° C. 29 g. of precipitate is obtained. This is slurried in 300 ml.of water, the pH adjusted to 8-8.5 with sodium hydroxide solution, the slurry heated to boiling and filtered. Cooling the filtrate gives 18 g. ofessentially pure product melting at 243°-244° C., as in the previous preparation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03992446 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-d9c4bbd8bd1145f7b1f71b9a3fd3383e |
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| Source note | uspto-grants-1976_11 |
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