HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507328Generated: November 2, 2026
Sodium Bicarbonate → 1-Acetyl-4,6-dimethylindoline
https://huagongshe.com/reaction/507328
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 4,6-dimethyl-1H-indole | HCID 9833991 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-Acetyl-4,6-dimethylindoline | HCID 9855693 | — |
Reaction Steps
4,6-Dimethylindole (1.08 g) was dissolved in acetic acid (20 ml), and sodium cyanoborohydride (2.3 g) was added portionwise at 15° C. The mixture was stirred at said temperature for one hour and poured into ice water. Saturated aqueous sodium bicarbonate was added to neutralize the mixture and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried over sodium sulfate. The solvent was evaporated under reduced pressure. The residue was dissolved in benzene, and acetic anhydride (840 mg) was added, which was followed by stirring at room temperature for one hour. The reaction mixture was washed with saturated aqueous sodium bicarbonate and saturated brine, and dried over sodium sulfate. The solvent was evaporated under reduced pressure. The residue was chromatographed (ISCO, hexane/EtOAc, 0-40%, 40 min) to give 1.3 g of 1-acetyl-4,6-dimethylindoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07786146B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-78222f0fd9624fde88fc2b1240752a9e |
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| Source note | uspto-grants-2010_08 |
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