HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55474Generated: October 29, 2026
Dimethylformamide → Methyl (2,3-dihydro-1H-indol-1-yl)acetate
https://huagongshe.com/reaction/55474
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Indoline | HCID 10328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl (2,3-dihydro-1H-indol-1-yl)acetate | HCID 22199910 | — |
Reaction Steps
0.40 ml of methyl bromoacetate was added dropwise to a mixture of 0.25 g of indoline, 2 ml of dimethylformamide and 0.87 g of anhydrous potassium carbonate, and the resulting mixture was stirred at room temperature for 1 hour. At the end of this time, the reaction mixture was poured into water, after which it was extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure, and the resulting residue was purified by column chromatography through silica gel, using a 5:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 0.30 g of the title compound having Rf=0.63 (on silica gel thin layer chromatography using a 2:1 by volume mixture of hexane and ethyl acetate as the developing solvent).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05624935 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-e52a6417b2a644ad95dfade076722b95 |
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| Source note | uspto-grants-1997_04 |
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