HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14159Generated: October 25, 2026
Sodium cyanoborohydride → Methyl 1-butylindoline-6-carboxylate
https://huagongshe.com/reaction/14159
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | methyl 1-butyl-1H-indole-6-carboxylate | HCID 21086134 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Methyl 1-butylindoline-6-carboxylate | HCID 21086137 | 77.4% |
Reaction Steps
To a mixture of methyl 1-butyl-1H-indole-6-carboxylate, (2.1 g) in glacial acetic acid (25 mL) was added sodium cyanoborohydride (2.28 g). The mixture was heated at 40° C. for 3 h then cooled to room temperature, partitioned between water and ethyl acetate and the layers were separated. The organic layer was washed three times with brine, dried over anhydrous sodium sulfate and concentrated to give 1.64 g of the title compound: 1H NMR (CDCl3) δ 0.969, 1.43, 1.59, 2.99, 3.1, 3.4, 3.88, 7.07, 7.34.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07727997B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-ec36e4517aeb4f9583456d798cf68415 |
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| Source note | uspto-grants-2010_06 |
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