HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole → 159884-46-5
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole | HCID 798 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 159884-46-5 | HCID 22013069 | — |
Reaction Steps
To a solution of 12 g of indole in 100 ml of dimethyl sulfoxide was added 6.5 g of sodium hydride at room temperature. The mixture was stirred at the same temperature for 1 hour, and 20 ml of bromoacetaldehyde diethyl acetal was added thereto, followed by further stirring at 50° C. for 1 hour. After cooling, the reaction mixture was poured into water, and the product was extracted with ethyl ether. The organic layer was dried over anhydrous magnesium sulfate and concentrated to give 23 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06207836B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-b538f0320d17460bb33b8d32030581c1 |
| Source note | uspto-grants-2001_03 |