HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526307Generated: October 26, 2026
Water → 1-(tert-Butyloxycarbonyl-methyl)-1H-indole-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/526307
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl indole-2-carboxylate | HCID 73125 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(tert-Butyloxycarbonyl-methyl)-1H-indole-2-carboxylic acid ethyl ester | HCID 54347069 | — |
Reaction Steps
A mixture of ethyl 1H-indole-2-carboxylate (5.68 g, 30 mmol), tert-butyl 2-bromoacetate (6.44 g, 33 mmol), and potassium carbonate in 60 mL of DMF was heated to 80° C. for 2 days. The TLC showed that the reaction stopped at around 50% completion. The reaction was worked up by the addition of water and the aqueous phase was extracted with EtOAc (2×30 mL). The combined organic phase was washed with brine, dried over Na2SO4, filtered and evaporated. The residue was purified by Combiflash (40 g silica gel cartridge, 0-30% EtOAc in hexane) to afford the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09345905B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-56d32c3a30314fe79858f9a356bb728b |
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| Source note | uspto-grants-2016_05 |
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