Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | (E)-Methyl 4-(2-(dimethylamino)vinyl)-3-nitrobenzoate | HCID 894337 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl indole-6-carboxylate | HCID 639844 | 39.9% |
Reaction Steps
To a mixed solvent of tetrahydrofuran (30 ml), ethanol (30 ml) and water (100 ml), added are methyl E-4-(2-dimethylaminovinyl)-3-nitrobenzoate (10.0 g) and sodium hydrosulfite (104.5 g), and stirred at 70° C. for 1 hours. After this is cooled to room temperature, a saturated saline solution is added thereto. Then, this is extracted with chloroform. The organic layer is dried, and the solvent is evaporated away. The resulting residue is purified through silica gel column chromatography (eluent: hexane/ethyl acetate=2/1 to 1/1) to obtain 6-methoxycarbonylindole (2.79 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115647B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-c315ac36537f4e9db6abb6977f887501 |
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| Source note | uspto-grants-2006_10 |
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