HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 5-Chloro-3-iodobenzene-1,2-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Chloro-2-iodo-6-nitroaniline | HCID 12143564 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | 5-Chloro-3-iodobenzene-1,2-diamine | HCID 54015998 | 96.3% |
Reaction Steps
1.5 g of 4-chloro-2-iodo-6-nitroaniline together with 50 ml of tetrahydrofuran and 10 ml of 1-propanol are initially introduced into a stirred autoclave. 5 mg of FeCl2.4H2O and 0.3 g Pt/Pb-CaCO3 catalyst are added to the solution, and hydrogenation is carried out at 130° C. and 20 bar of hydrogen. After the hydrogenation has come to a standstill, the reaction mixture is cooled to room temperature, the reactor is rendered inert with nitrogen and the catalyst is filtered off. After filtration, the solvent is removed by distillation to give 1.3 g of 4-chloro-6-iodo-1,2-phenylenediamine as a crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05877340 |
| Source dataset | uspto-grants-1999_03 |
| ORD ID | ord-a96c476860a947fe84554ab6a145ed73 |
| Source note | uspto-grants-1999_03 |