HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131641Generated: October 25, 2026
Ethyl Acetate → Ethyl 5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxylate
https://huagongshe.com/reaction/131641
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-Fluorobenzyl chloride | HCID 9974 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | ethyl 5-fluoro-1H-indole-2-carboxylate | HCID 2727899 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxylate | HCID 57431514 | 61.8% |
Reaction Steps
A suspension of 0.207 g (1 mmol) of ethyl 5-fluoro-1H-indole-2-carboxylate, 0.173 g (1.2 mmol) of 3-fluorobenzyl chloride and 0.276 g (2 mmol) of potassium carbonate in 10 ml of dimethylformamide is stirred at 60° C. for 24 hours. The reaction mixture is subsequently cooled and is poured into a mixture of ice-cold water and of ethyl acetate. After settling, the organic phase is separated and then it is washed with two times 50 ml of water and then with 50 ml of a saturated sodium chloride solution. The solution is dried over magnesium sulfate and is filtered, and then the filtrate is concentrated under reduced pressure. 0.195 g of an oil is obtained, which oil is used as is in the following stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07384969B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-276fbec6c06f45fea6c86055a2670eef |
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| Source note | uspto-grants-2008_06 |
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