HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158385Generated: November 1, 2026
Water → Methyl 3-methyl-1H-indole-6-carboxylate
https://huagongshe.com/reaction/1158385
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 | — |
Reaction Steps
A mixture of 3-formyl-1H-indole-6-carboxylic acid methyl ester (5 g, 24.6 mmol), p-toluene-sulfonic acid (704 mg, 3.7 mmol) and p-toluenesulfonylhydrazide (5.49 g, 29.5 mmol) in a mixture of dimethylformamide (50 mL) and sulfolane (25 mL) is heated at 100° C. for 15 min. Then cooled to RT, before the addition of sodium cyanoborohydride (6.2 g, 98.4 mmol, 2 g portions after 10 min intervals). The resulting mixture is heated at 100° C. for 2 h, cooled to RT and poured into a mixture of ice and water (250 mL) leading to a white precipitate. Water (500 mL) is added, and the mixture is stirred for 30 min before filtration. The off-white solid is washed with warm water. Toluene is added and removed by rotary evaporation to afford the title compound as a yellow solid. TLC, Rf (hexane/AcOEt 4:1)=0.3. MS (LC-MS): [M+H]+=188.1. tR (HPLC, Macherey-Nagel Nucleosil C18 column, 10-100% CH3CN/H2O/5 min, 100% CH3CN/3 min, CH3CN and H2O containing 0.1% TFA, flow: 1.5 mL/min): 5.13 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07807709B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-db66c2cba08d420c84ec73a40f7af56e |
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| Source note | uspto-grants-2010_10 |
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