HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Chloride → HCID 68052643, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | HCID 86651927 | HCID 86651927 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68052643 | HCID 68052643 | — |
Reaction Steps
To a mixture of N,2-bis(2,4-dimethoxybenzyl)-6-nitroisoindolin-5-amine T-03 (2.7 g, 5.6 mmol) and sodium hydrosulfite (15.6 g, 90 mmol) was added a solution of tetrahydrofuran (40 mL), water (40 mL) and ammonium hydroxide (40 mL). The reaction mixture was stirred at room temperature overnight. The reaction mixture was basified with sodium hydroxide and saturated with sodium chloride. The reaction mixture was filtered and extracted with ethyl acetate. The organic layer was dried over sodium sulfate. Solvent was evaporated under reduced pressure to afford the desired N5,2-bis(2,4-dimethoxybenzyl)isoindoline-5,6-diamine T-04 (2.5 g, 5.6 mmol). The crude product was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08148363B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-a6a1f82423ca4f9e9f97f68e8506e455 |
| Source note | uspto-grants-2012_04 |