HuagongsheHuagongshe Chemistry Print Report · For research reference only
Guanidine → Diaveridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Guanidine | HCID 3520 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | alpha-Carbethoxy-alpha-diethoxymethyl-beta-(3,4-dimethoxyphenyl)propionitrile | HCID 12559142 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Diaveridine | HCID 21453 | 54% |
Reaction Steps
A solution of α-carbethoxy-α-diethoxymethyl-β-(3,4-dimethoxyphenyl)-propionitrile (3.75 g) and an equivalent amount of potassium hydroxide in ethanol (70 ml) was heated at reflux for one hour. A solution of guanidine (0.035 mol) in ethanol (50 ml) was added and reflux was resumed. Ethanol was boiled off until the reaction temperature reached 85° C. After 17 hours at reflux the mixture was allowed to cool and the product was filtered and washed with ethanol giving a white solid which was purified as described in Example 5 to yield 1.4 g (54%) of the title compound, m.p. 231°-233° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04144263 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-101a4f15dee1482f914ef453c0032123 |
| Source note | uspto-grants-1979_03 |