HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 6-Iodoindoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Acetyl-6-iodoindoline | HCID 11666396 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Iodoindoline | HCID 11615696 | 64% |
Reaction Steps
1-Acetyl-6-iodoindoline (1.06 g, 3.7 mmol), NaOH (1.16 g, 29 mmol), EtOH (8 mL), and H2O (6 mL) are heated at 90° C. overnight. The reaction mixture is then partitioned between H2O and EtOAc. The organic layer is extracted into aqueous HCl. The aqueous layer is in turn basified with NaOH, and is extracted with EtOAc. The organic layer is dried and concentrated. Hexane trituration yields 6-iodoindoline (577 mg, 64%) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07868037B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-a0f13259a14d43c5b16fbd2049ae4af8 |
| Source note | uspto-grants-2011_01 |