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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941028Generated: November 2, 2026

Water → HCID 21459470, compound

https://huagongshe.com/reaction/1941028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantHCID 21459436HCID 21459436—
SolventDichloromethaneHCID 6344—
ProductHCID 21459470HCID 21459470—

Reaction Conditions

Temperature0 °C

Reaction Steps

The above 2-(4-(1,4-dioxaspiro[4.5]decyl)cyclohexyl)ethanol (20 g, 70.8 mmol) was dissolved in dichloromethane (70 ml), followed by dropwise adding to the solution, DAST (13 g, 80.7 mmol), stirring at 0° C. for one hour, adding water to the reaction solution, washing the resulting organic layer successively with a saturated aqueous solution of sodium bicarbonate and water, distilling off the solvent, purifying the residue according to column chromatography using heptane/ethyl acetate as a developing solvent, on silica gel, to obtain 1-(4-(1,4-dioxaspiro[4,5]decyl)cyclohexyl)-2-fluoroethane, adding thereto formic acid (80 ml), refluxing the mixture for 2 hours, extracting the resulting product with toluene, washing the extraction solution successively with a saturated aqueous solution of sodium bicarbonate, distilling off the solvent, to isolate 4-(4-(2-fluoroethyl)cyclohexyl)cyclohexanone (8.0 g, 35.3 mmol). The yield of this product from 2-(4-(1,4-dioxaspiro[4,5]decyl)cyclohexyl)ethanol was 49.9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05702641
Source datasetuspto-grants-1997_12
ORD IDord-c32ab3997d5f4d3798b79f48f9acfb18
Source noteuspto-grants-1997_12