Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 18325143 | HCID 18325143 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18325115 | HCID 18325115 | 125.7% |
Reaction Steps
To a suspension of lithium aluminum hydride (180 mg) in THF (15 ml), ethyl 3-ethoxycarbonylmethyl-4-(4-fluorophenyl)-6-methoxyquinoline-2-carboxylate (1.0 g) was added, followed by stirring at 0° C. for 30 minutes. Water was added to the reaction mixture to stop the reaction; after the insoluble substances were filtered off, the product was extracted with ethyl acetate. After being washed with water, the extract was dried over magnesium sulfate and concentrated under reduced pressure to yield a crude crystal (1 g) of the title compound. The crude crystal obtained was used for the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06340704B1 |
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| Source dataset | uspto-grants-2002_01 |
|---|
| ORD ID | ord-afe4b084417e4296ab800f15bfe78fcd |
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| Source note | uspto-grants-2002_01 |
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