HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888911Generated: October 27, 2026
Water → Methyl 5-fluoro-1H-indole-3-carboxylate
https://huagongshe.com/reaction/888911
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 5-Fluoroindole | HCID 67861 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 5-fluoro-1H-indole-3-carboxylate | HCID 34176452 | 83% |
Reaction Steps
A solution of 5-fluoroindole (5 g, 37.0 mmol) in DMF (40 mL) was treated at 0° C. with trifluoroacetic anhydride (6.1 mL, 42.6 mmol). After 30 min, the reaction was poured into water and the resulting precipitate collected by filtration, washed with water, then dried in vacuo. The solid was then dissolved in 10% aqueous NaOH (200 mL) and heated at reflux for 1 h. The reaction mixture was then cooled, washed with dichloromethane and acidified with aqueous HCl. The resulting white precipitate was collected by filtration, washed with water, taken up in dichloromethane, washed with water, dried (MgSO4) and evaporated in vacuo. The resulting material (5 g, 75%) was dissolved in methanol (80 mL) and treated with concentrated sulphuric acid (2 mL) then heated at reflux overnight. The reaction was cooled and the resulting precipitate collected, washed with water and evaporated in vacuo to give 5-fluoro-1H-indole-3-carboxylic acid methyl ester as a peach-coloured solid (4.5 g, 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08252792B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-55bef237fcba4c5aad862f7ea09d0f45 |
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| Source note | uspto-grants-2012_08 |
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