HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854671Generated: November 1, 2026
Indole-3-Carboxaldehyde → HCID 13979912, compound
https://huagongshe.com/reaction/1854671
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Indole-3-Carboxaldehyde | HCID 10256 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 13979912 | HCID 13979912 | 65% |
Reaction Steps
To a solution of 1H-indole-3-carboxaldehyde (300 mg, 2.07 mmol) in 4.1 mL of dry dimethylsulfoxide was added sodium hydride (108 mg, 55%, 2.5 mmol) under nitrogen at 0° C. After the reaction mixture was stirred for 30 min, methylsulfonyl chloride (0.19 mL, 2.5 mmol) was added with additional stirring for 1 h. The reaction mixture was diluted with 10 mL of ethyl acetate and 10 mL of saturated NH4Cl aqueous solution at 0° C., successively, and the solution was extracted with 100 mL of ethyl acetate. The extract was washed with saturated NaHCO3 aqueous solution, brine, and dried over MgSO4. After filtration, the solution was concentrated in vacuo. The residue was purified by recrystallization (chloroform/hexane) to obtain the title compound as a pale red solid (300 mg, 65%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962674B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-78b62b6adb0c4affaafc71937ae2e557 |
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| Source note | uspto-grants-2015_02 |
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