HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887203Generated: October 29, 2026
Sodium cyanoborohydride → 6-Bromo-2,3-dihydro-5-methyl-1H-indole
https://huagongshe.com/reaction/1887203
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 6-bromo-5-methyl-1H-indole | HCID 10750926 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-Bromo-2,3-dihydro-5-methyl-1H-indole | HCID 18940918 | 71.1% |
Reaction Steps
A solution of 6-bromo-5-methylindole (1.00 g, 4.75 mmol) in AcOH (150 mL) was treated with NaBH3CN (0.897 g, 14.3 mmol) while maintaining a temperature of −10° C. The mixture was then stirred at RT overnight and concentrated. The resulting residue was treated with aqueous K2CO3, and extracted with DCM (3×100 mL). The combined organic layers were dried over MgSO4, concentrated and purified by column chromatography (0-75% EtOAc/hexanes) to afford 6-bromo-5-methylindoline (13A, 716 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501747B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-828da0fa6ef946e282415e803e7bdf80 |
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| Source note | uspto-grants-2013_08 |
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