HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 70621761, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | HCID 20352737 | HCID 20352737 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 70621761 | HCID 70621761 | — |
Reaction Steps
To 2.89 gms. (0.01 mole) of 1-(p-trifluoroacetamidophenyl)-3-methyl-3-(4-pyridylmethyl)urea [prepared by reacting 1-(p-aminophenyl)-3-methyl-3-(4-pyridylmethyl)urea (Example 6., supra.) with trifluoroacetic anhydride (method of Hickenbottom, Reactions of Organic Compounds, Longmans, London, 1963)] there is added 6.24 gms. (0.04 mole) of ethyl iodide in 50 ml. of dry acetone. The acetone is then stripped and the residue added to 50 ml. of water. The aqueous mixture is warmed to reflux for about 30 minutes and then allowed to stand overnight. The mixture is then stripped of water to give 1-(p-ethylaminophenyl)-4-methyl-3-(4-pyridylmethyl)urea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04088766 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-c4a626f71b514849a382a40b09a0abde |
| Source note | uspto-grants-1978_05 |