HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859243Generated: October 26, 2026
Potassium Carbonate → Ethyl 2-(2-fluoroethyl)-5-methoxy-1-oxoindane-2-carboxylate
https://huagongshe.com/reaction/859243
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Fluoroethyl bromide | HCID 12982 | — |
| Reactant | ethyl 5-methoxy-1-oxo-2,3-dihydro-1H-indene-2-carboxylate | HCID 12177975 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Ethyl 2-(2-fluoroethyl)-5-methoxy-1-oxoindane-2-carboxylate | HCID 16726730 | — |
Reaction Steps
To a mixture of ethyl 5-methoxy-1-oxoindane-2-carboxylate (crude product from the preceding two reactions, ˜190 mmol), K2CO3 (53.8 g, 389 mmol) and KI (64.7 g, 390 mmol) in anhydrous dimethylacetamide (792 mL) was added 1-bromo-2-fluoroethane (18.4 mL, 247 mmol) and the mixture was stirred and heated at 65° C. After 20 hours, analysis of an aliquot by NMR showed the reaction to be complete. After cooling to room temperature, most of the dimethylacetamide was removed by evaporation at reduced pressure. The residue was partitioned between EtOAc and water and the organic phase was washed with water (4 times) and brine and dried over Na2SO4. Filtration and removal of the solvent under reduced pressure gave crude ethyl 2-(2-fluoroethyl)-5-methoxy-1-oxoindane-2-carboxylate which was used in the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07151196B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-2b2bb60d002a4136a34f1ac72f33e75f |
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| Source note | uspto-grants-2006_12 |
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