HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23414Generated: October 27, 2026
Hydrochloric Acid → 6-Bromo-1-cyanomethyl-1H-indole-3-carboxylic Acid
https://huagongshe.com/reaction/23414
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Bromo-1H-indole-3-carboxylic acid | HCID 15284837 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Bromo-1-cyanomethyl-1H-indole-3-carboxylic Acid | HCID 22574082 | 68% |
Reaction Steps
6-Bromo-1H-indole-3-carboxylic acid (0.24 g, 1 mmole) was dissolved in anhydrous dimethylformamide (2 ml) and cooled to 0° C. in a nitrogen atmosphere. With stirring, sodium hydride (60% in oil, 0.088 g, 2.2 mmole) was added all at once and the mixture was stirred at this temperature until no more bubbles evolved (ca. 20-30 minutes). Bromoacetonitrile (0.132 g, 1.1 mmole) was added to the reaction mixture which was then allowed to warm to room temperature over the next hour. The reaction mixture was poured into water, acidified with HCl and a precipitate formed. When dried the product weighed 0.190 g (68% yield) and was sufficiently pure to be used directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06852726B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-e4124114688942ac9062624f8cc731ac |
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| Source note | uspto-grants-2005_02 |
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