HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260833Generated: October 26, 2026
Ethyl 4-bromobutyrate → Ethyl 4-(3-benzyloxycarbonyl-1-indolyl)-butyrate
https://huagongshe.com/reaction/260833
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Reactant | benzyl 1H-indole-3-carboxylate | HCID 8605861 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 4-(3-benzyloxycarbonyl-1-indolyl)-butyrate | HCID 22400494 | — |
Reaction Steps
A mixture of benzyl indole-3-carboxylate, ethyl 4-bromobutyrate and potassium t-butoxide in N,N-dimethylformamide was stirred at 50° C. for 4 hours. After insoluble materials were filtered off, the filtrate was diluted with ethyl acetate, and washed with diluted hydrochloric acid and water, dried over magnesium sulfate and concentrated. The concentrate was chromatographed on a silica gel column to give the object compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05530019 |
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| Source dataset | uspto-grants-1996_06 |
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| ORD ID | ord-bea85c6851bd439881b44c9c5a4c9fcc |
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| Source note | uspto-grants-1996_06 |
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