HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 1H-Indole-7-carboxaldehyde, 3-iodo-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Indole-7-carboxaldehyde | HCID 2734629 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1H-Indole-7-carboxaldehyde, 3-iodo- | HCID 59541434 | — |
Reaction Steps
To a starting material (indole-7-carbaldehyde), a solution of 24 g of I2 in 125 ml of DMF (dimethylformamide) was added with stirring, and 5.3 g of KOH was added, after which the mixture was allowed to react. The termination of the reaction was confirmed with thin layer chromatography (TLC), after which layer separation was conducted with 354 ml of EA and 354 ml of purified water. The organic layer was washed with aqueous 10% Na2S2O3, dried with Na2SO4 (sodium sulfate), filtered and concentrated at 40, thus obtaining P10 as a concentrated residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08940739B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-7c85cfffad7d4df7bc8cd2d223882873 |
| Source note | uspto-grants-2015_01 |