HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → HCID 178424782, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,6-Dimethylbenzaldehyde | HCID 583841 | — |
| Reactant | HCID 178506603 | HCID 178506603 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178424782 | HCID 178424782 | — |
Reaction Steps
A solution of 1.34 g. of 2,6-dimethylbenzaldehyde [G. Lock and K. Schmidt, J. Prakt. Chem., 140, 229 (1934) and 2.92 g. of 1-amino-3-benzylguanidine hydroiodide in 25 ml. of absolute ethanol is heated at reflux for 18 hours. The solution is evaporated under reduced pressure to give a syrup which is made alkaline with aqueous NaOH. The mixture is extracted with chloroform. The chloroform extract is evaporated under reduced pressure to give a yellow syrup. Trituration of this syrup with diethyl ether and n-hexane, followed by filtration, gives the desired product as light pink crystals, m.p. 125°-126° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04107326 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-c2450ed3a34840309f1947b44d0b79e0 |
| Source note | uspto-grants-1978_08 |