HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948145Generated: October 31, 2026
Sodium Bicarbonate → 4-Oxo-1-(tetrahydro-2H-pyran-4-yl)cyclohexanecarbonitrile
https://huagongshe.com/reaction/1948145
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 8-(Tetrahydropyran-4-yl)-1,4-dioxa-spiro[4.5]decane-8-carbonitrile | HCID 67072827 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 4-Oxo-1-(tetrahydro-2H-pyran-4-yl)cyclohexanecarbonitrile | HCID 58380823 | 70.4% |
Reaction Steps
A solution of 10.3 g (40.8 mmol) of 8-(tetrahydropyran-4-yl)-1,4-dioxa-spiro[4.5]decane-8-carbonitrile (5) in a mixture of 90 mL of acetic acid and 18 mL of water was heated at 100° C. for 24 h. The mixture was cooled to room temperature and slowly poured onto 1.2 L of cold saturated aqueous sodium bicarbonate solution. The mixture was diluted with 600 mL of brine and extracted six times with methyl-tert-butyl ether. The combined organic phases were washed with water and brine, dried over magnesium sulphate, filtered and concentrated in vacuo. The residue was lyophilized from acetonitrile and water, taken up in water and lyophilized again to give 5.95 g of the ketone, which was used directly in the next step. Rt=0.82 min (Method O). Detected mass: 208.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399482B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-1591b97b721341febfc04ee79fd2016f |
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| Source note | uspto-grants-2013_03 |
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