HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015980Generated: October 31, 2026
Sodium Bicarbonate → 4-(1-Hydroxy-4-oxocyclohexyl)benzonitrile
https://huagongshe.com/reaction/1015980
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-(8-Hydroxy-1,4-dioxaspiro[4.5]decan-8-yl)benzonitrile | HCID 15023905 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(1-Hydroxy-4-oxocyclohexyl)benzonitrile | HCID 66787229 | 95.2% |
Reaction Steps
4-(8-Hydroxy-1,4-dioxaspiro[4.5]dec-8-yl)benzonitrile (520 mg, 2.0 mmol) was dissolved in the mixed solvent of 10 mL of THF and 10 mL of 1 N HCl aqueous solution at room temperature. The reaction mixture was then stirred at 60° C. for 1 h. The solution was cooled down to room temperature, adjusted to pH 7-8 with saturated NaHCO3 aqueous solution. The organic layer was separated, and the aqueous layer was extracted twice with EtOAc (20 mL×2). The combined organic extracts were dried over MgSO4 and evaporated to give an oil residue. Chromatography on silica gel (flash chromatography grade) with 40% ethyl acetate-hexane gave 410 mg (95%) of the desired product: 1H NMR (CDCl3) δ 7.7 (2H, d, J=11.0 Hz), 7.42 (2H, d, J=10.7 Hz), 4.10 (H, s), 2.79-2.74 (2H, m), 2.63-2.49 (2H, m), 1.95-1.89 (2H, m), 1.67-1.59 (2H, m); MS: 216 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985730B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-6bf26003771a42aca5c9e1274e084b21 |
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| Source note | uspto-grants-2011_07 |
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