HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 1-(1,3-Benzodioxol-5-yl)-1-isopropylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | NaNCO | HCID 11051568 | — |
| Reactant | N-(Propan-2-yl)-2H-1,3-benzodioxol-5-amine | HCID 12789466 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-(1,3-Benzodioxol-5-yl)-1-isopropylurea | HCID 100555 | — |
Reaction Steps
To a solution of 14.7 gm. of N-isopropyl-3,4-methylenedioxyaniline, prepared as in Example A, in 200 ml. of glacial acetic acid, cooled to 10°-18°C., is added 4.9 gm. of sodium isocyanate (sodium cyanate) in several portions. The resulting mixture is then stirred at ambient temperature for 15 hours. At the end of this time, the solvent is stripped at reduced pressure and the solid residue treated with 300 ml. of 2N sodium hydroxide. The resulting mixture is extracted with chloroform, dried and evaporated. The gum thus obtained is recrystallized from cyclohexane to obtain N-isopropyl-N-(3,4-methylenedioxyphenyl)urea, m.p. 116°-119°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03997564 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-19a415d1e1514a3a9c8c6864e05ef80b |
| Source note | uspto-grants-1976_12 |