HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aluminium lithium hydride → [5-(2-morpholin-4-yl-ethoxy)-1H-indol-2-yl]-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 5-(2-morpholin-4-yl-2-oxo-ethoxy)-1H-indole-2-carboxylic acid ethyl ester | HCID 69587391 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [5-(2-morpholin-4-yl-ethoxy)-1H-indol-2-yl]-methanol | HCID 22042178 | 105.5% |
Reaction Steps
Lithium aluminum hydride (0.46 g, 12 mmol) was added 5-(2-morpholin-4-yl-2-oxo-ethoxy)-1H-indole-2-carboxylic acid ethyl ester (0.8 g, 2.4 mmol) in tetrahydrofuran (50 mL). The mixture was stirred at room temperature for 16 hours and cooled to 0° C. It was then quenched with water (4.6 mL), 15% sodium hydroxide (4.6 mL) and water (4.6 mL). The precipitate was filtered off and the filtrate was concentrated to give 0.7 g of [5-(2-morpholin-4-yl-ethoxy)-1H-indol-2-yl]-methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07071332B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-5e1c4064a4ed436997c164f1d796bf87 |
| Source note | uspto-grants-2006_07 |