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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant8-(Tetrahydropyran-4-yl)-1,4-dioxa-spiro[4.5]decane-8-carbonitrileHCID 67072827—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventSodium chloride; waterHCID 57417360—
Product4-Oxo-1-(tetrahydro-2H-pyran-4-yl)cyclohexanecarbonitrileHCID 5838082370.4%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399482B2
Source datasetuspto-grants-2013_03
ORD IDord-1591b97b721341febfc04ee79fd2016f
Source noteuspto-grants-2013_03