HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278131Generated: October 31, 2026
Sodium borohydride → HCID 22627373, compound
https://huagongshe.com/reaction/278131
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22627257 | HCID 22627257 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22627373 | HCID 22627373 | 39.8% |
Reaction Steps
To a solution of 1-(2-chlorobenzyl)-3-isobutyryl-2-propylindole-6-carbonitrile (70 mg) in a mixture of methanol (2 ml) and tetrahydrofuran (2 ml) was added sodium borohydride (21 mg) at 25° C. After stirred at 25° C. for 2 hours, the reaction mixture was partitioned between ethyl acetate and 1N hydrochloric acid. The organic layer was washed with water and brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was crystallized from diisopropyl ether to give 1-(2-chlorobenzyl)-3-(1-hydroxy-2-methylpropyl)-2-propylindole-6-carbonitrile (28 mg) as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06358992B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-9a5b5f5a8ef943aaab82350bbbdb01b9 |
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| Source note | uspto-grants-2002_03 |
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