HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 178512115, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2,6-Dichlorobenzaldehyde | HCID 6737 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178506605 | HCID 178506605 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178512115 | HCID 178512115 | — |
Reaction Steps
A solution of 1.75 g. of 2,6-dichlorobenzaldehyde and 2.82 g. of 1-amino-3-furfurylguanidine hydriodide in 15 ml. of glacial acetic acid is heated at 100° C. for one hour, cooled, and diluted with absolute ether until crystallization occurs. Filtration gives 3.51 g. of gray-colored crystals. The crystals are dissolved by warming in absolute ethanol and the solution is treated with excess 10N sodium hydroxide and diluted with water to turbidity. Chilling and filtration give 2.00 g. of nearly colorless crystals. Two recrystallizations from aqueous ethanol, using activated charcoal, give the desired product as colorless crystals, m.p. 134°-135.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04154947 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-f2f5f739fc294997b70d42275b177bfb |
| Source note | uspto-grants-1979_05 |