HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32049Generated: October 27, 2026
Sodium borohydride → 7-Cyano-4-chromanol
https://huagongshe.com/reaction/32049
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-Cyano-4-chromanone | HCID 22349973 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-Cyano-4-chromanol | HCID 18448612 | — |
Reaction Steps
7-Cyano-4-chromanone (Step A) (7.7 g, 44 mmol) was dissolved in THF (75 mL) and MeOH (150 mL), and cooled to 10° C. NaBH4 (1.9 g, 49 mmol) was added and the reaction was warmed to RT and stirred overnight (14 h). The reaction was quenched with acetone (5 mL) and 2 N HCl (100 mL) was added. The reaction was concentrated in vacuo to approximately 75 mL in volume and the reaction was partitioned between 2N HCl (200 mL) and EtOAc (400 mL). The layers were separated and the aqueous layer was back extracted with EtOAc (200 mL). The organic layers were combined, washed successively with H2O (200 mL) and brine (200 mL). The solution was dried over MgSO4, filtered and concentrated in vacuo to provide the title compound which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07425631B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-6bc56a94342f4632a906bd37fc714ea7 |
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| Source note | uspto-grants-2008_09 |
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