HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392233Generated: October 25, 2026
Ammonia → 5-trifluoromethoxy-1H-indole-2-carboxylic acid amide
https://huagongshe.com/reaction/1392233
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 5-(Trifluoromethoxy)-1H-indole-2-carboxylic acid | HCID 2777290 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-trifluoromethoxy-1H-indole-2-carboxylic acid amide | HCID 69220468 | — |
Reaction Steps
Oxalyl chloride (2.63 ml, 30.6 mmol) was added dropwise at 0° C. within 45 min. to a suspension of 5-trifluoromethoxy-1H-indole-2-carboxylic acid (5 g, 20.4 mmol) in THF (20 ml) and N,N-dimethyl formamide (0.5 ml). Stirring was continued at 0-5° C. for 30 min. and thereafter for 3 h at room temperature. The resulting solution was cooled to 0-5° C. again and then added within 15 min. to 75 ml of a 25% aqueous solution of ammonia. After stirring for 30 min. the precipitated amide was collected, washed with water and dried at 40° C. in vacuo yielding 5-trifluoromethoxy-1H-indole-2-carboxylic acid amide as off white solid. Yield 5 g (100%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07342030B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-1dacd341192f45c2af9a533f0eb0a81b |
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| Source note | uspto-grants-2008_03 |
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