HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600611Generated: October 29, 2026
tert-Butyl acrylate → ethyl 1-(2-tert-butoxycarbonylethyl)-4-methyl-1H-indole-2-carboxylate
https://huagongshe.com/reaction/1600611
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butyl acrylate | HCID 15458 | — |
| Reactant | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| Reactant | Ethyl 4-methyl-1H-indole-2-carboxylate | HCID 12529972 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | ethyl 1-(2-tert-butoxycarbonylethyl)-4-methyl-1H-indole-2-carboxylate | HCID 15548944 | 87% |
Reaction Steps
A mixture of ethyl 4-methyl-1H-indole-2-carboxylate (70.0 g, 344 mmol), tert-butyl acrylate (53.0 g, 413 mmol), benzyltrimethylammonium hydroxide (5.76 g, 34.4 mmol) and 1,4-dioxane (1,000 ml) was stirred at 60-62° C. for 8.5 hours. The solvent was distilled off under reduced pressure and water (1,000 ml) and acetic acid. (30 ml) were added to the residue, followed by extraction with ethyl acetate (twice). The extract solution was washed with a 5% aqueous sodium hydrogencarbonate solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was crystallized from isopropanol (230 ml) to obtain ethyl 1-(2-tert-butoxycarbonylethyl)-4-methyl-1H-indole-2-carboxylate (99.2 g). M.p. 78-79° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05977100 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-6fab74eec8664dc3abf0785da87eaa25 |
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| Source note | uspto-grants-1999_11 |
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