HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74523Generated: October 26, 2026
Sodium cyanoborohydride → HCID 58386466, compound
https://huagongshe.com/reaction/74523
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 3-(3-pyrrolidin-1-yl-propyl)-1H-indole | HCID 58386508 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 58386466 | HCID 58386466 | — |
Reaction Steps
At 15° C. 508 mg (8.10 mmol) sodium cyanoborohydride was added to 600 mg (2.63 mmol) 3-(3-pyrrolidin-1-yl-propyl)-1H-indole in 7.50 g acetic acid and the mixture was stirred for 1 h at 15° C. After this time another 600 mg sodium cyanoborohydride were added and the mixture was stirred at 15° C. for 3 h. The reaction mixture was evaporated down using the rotary evaporator and combined with 40 mL of a 4M hydrochloric acid solution. The reaction mixture was stirred for 1h at RT. Then the mixture was made basic with potassium carbonate and extracted with ethyl acetate (2×50 mL). The combined organic phases were dried and evaporated down i. vac. The product was reacted further without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829006B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-a878730b334c4115b5d4b0b5490ed774 |
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| Source note | uspto-grants-2014_09 |
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