HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380427Generated: October 26, 2026
Water → Methyl 3-methyl-1H-indole-6-carboxylate
https://huagongshe.com/reaction/380427
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | methyl 3-formyl-1H-indole-6-carboxylate | HCID 735867 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Sulfolane | HCID 31347 | — |
| Product | Methyl 3-methyl-1H-indole-6-carboxylate | HCID 21938240 | 91.3% |
Reaction Steps
A mixture of methyl 3-formyl-1 H-indole-6-carboxylate (12.0 g), p-toluenesulphonic acid (2.0 g) and p-toluenesulphonylhydrazide (13.0 g) in a mixture of dimethylformamide (100 ml) and sulpholane (50 ml) was heated at 100° C. for 15 minutes and then cooled to room temperature. The mixture was treated with sodium cyanoborohydride (15.0 g, 5 g portions after 10 minute intervals), then heated at 100° C. for 2 hours. After cooling to ambient temperature the reaction mixture was treated with ice water (500 ml) giving a white precipitate. Water (1000 ml) was added and the mixture stirred for 30 minutes then filtered. The off-white solid was washed with warm water then azeotroped with toluene to yield the title compound (10.2 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06303600B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-903bc2518b1d41eead73bfbed94e71d9 |
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| Source note | uspto-grants-2001_10 |
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