Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Ethyl 5-(phenylmethoxy)-1H-indole-2-carboxylate | HCID 95721 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 76494514 | HCID 76494514 | — |
Reaction Steps
5-Benzyloxyindole-2-carboxylic acid ethylester (3 g, 10.1 mmol) and magnesium turnings (1.2 g, 50 mmol) were suspended in dried methanol (180 mL). This mixture was stirred at 5-10° C. under nitrogen for 3 hours, then poured into dichloromethane, and washed with saturated ammonium chloride solution. The organic layer was separated, and the aqueous layer was extracted with dichloromethane. The combined organic layers were dried over sodium sulphate and evaporated to leave a brown solid which was further purified by column chromatography (silica gel, dichloromethane) to afford a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06335360B1 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-ebc618a576fc48beab4b68a08290496d |
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| Source note | uspto-grants-2002_01 |
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