HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 5-tert.Butylcarbamylphthalid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 1,3-Dihydro-1-oxoisobenzofuran-5-carboxylic acid | HCID 78517 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | 5-tert.Butylcarbamylphthalid | HCID 11148992 | — |
Reaction Steps
5-Carboxyphthalid (36 g, 0.2 mole) is suspended in thionylchloride (100 mL). DMF (1.5 mL) is added and the mixture is refluxed for 1 hour. Toluene (200 mL) is added and the solvents are evaporated in vacuo. The residue is dissolved in THF (200 mL) and added to a solution of tert.butylamine (31 g, 0.42 mole) in THF (200 mL) at 5° C. The mixture is allowed to warm to room temperature and stirred overnight. The reaction is then poured into ice water (400 mL) and the precipitated crystals are filtered off. The crystals are washed with water (100 mL). Yield: 41 g, 87%. DSC onset: 189.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06229026B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-94938be2fcd0455e9ea8ccdb7d16aa64 |
| Source note | uspto-grants-2001_05 |