HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565061Generated: October 31, 2026
Stannous chloride dihydrate → Ethyl 7-(4-aminophenoxy)-4-chloro-1-methyl-2-indolecarboxylate
https://huagongshe.com/reaction/565061
Participants
| Role | Name | HCID | Charge |
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| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Reactant | HCID 21194161 | HCID 21194161 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 7-(4-aminophenoxy)-4-chloro-1-methyl-2-indolecarboxylate | HCID 21194433 | 71.8% |
Reaction Steps
A mixture of 4.10 g (10.9 mmol) of ethyl 4-chloro-1-methyl-7-(4-nitrophenoxy)-2-indolecarboxylate, 12.34 g (54.7 mmol) of tin (II) chloride dihydrate and 150 ml of ethanol was stirred at 70° C. for 3 hours. After the reaction mixture was cooled to room temperature, 28% ammonia water was added to render alkaline and the mixture was extracted with ethyl acetate. Insoluble matters were filtered off. The filtrate was washed with 5% sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography to give 2.70 g of ethyl 7-(4-aminophenoxy)-4-chloro-1-methyl-2-indolecarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06169107A |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-e8598d7f8f0a453aae2910b5a19101a7 |
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| Source note | uspto-grants-2001_01 |
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