HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → HCID 178453988, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | 3-Nitrophthalic anhydride | HCID 21631 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 178419079 | HCID 178419079 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178453988 | HCID 178453988 | 99.1% |
Reaction Steps
15 ml of a chloroform solution containing 500 mg of N-tert-butoxycarbonyl-trans-1,4-cyclohexanediamine and 540 mg of 3-nitrophthalic anhydride was refluxed for 1 hour. After cooling, 756 mg of carbonyldiimidazole was added to the mixture and the resulting mixture was stirred at room temperature for 15 hours. Water was added to the reaction mixture and the resulting mixture was extracted with chloroform. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The residue was purified by silica gel flash column chromatography to obtain 900 mg of N-tert-butoxycarbonyl-trans-4-(1,3-dioxo-4-nitro-2-isoindolinyl)cyclohexylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138397B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-f11f7765d906497d85dedb2c04e0064f |
| Source note | uspto-grants-2006_11 |