HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73569Generated: October 29, 2026
Sodium borohydride → HCID 59226486, compound
https://huagongshe.com/reaction/73569
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-(3-Nitropyridin-4-yl)cyclohex-2-enone | HCID 59226544 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59226486 | HCID 59226486 | 99% |
Reaction Steps
To a solution of 3-(3-nitropyridin-4-yl)cyclohex-2-enone (1.0 equiv.) was added EtOH (1.1M) and CeCl3-7H2O (1.3 equiv.). The reaction was cooled to 0° C., then NaBH4 (1.3 equiv.) was added in portions. Stirred for 2 h at 0° C., then quenched by adding water, concentrated to remove the EtOH, added EtOAc, extracted the organics, dried with brine, then Na2SO4, and concentrated to yield 3-(3-nitropyridin-4-yl)cyclohex-2-enol (99%). LC/MS=221.1 (M+H), LC=2.24 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829193B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-5d3ce4be06fd43e188e2e5f5a11ea8fc |
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| Source note | uspto-grants-2014_09 |
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