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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050455Generated: November 1, 2026

Water → 4-Oxocyclohexane-1-carbaldehyde

https://huagongshe.com/reaction/2050455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant8-(Methoxymethylene)-1,4-dioxaspiro[4.5]decaneHCID 55277137—
SolventAcetic AcidHCID 176—
Product4-Oxocyclohexane-1-carbaldehydeHCID 1117097393%

Reaction Steps

A mixture of 10.55 g of 1,1-ethylenedioxy-4-(methoxymethylene)cyclohexane, 130 ml of water and 200 ml of glacial acetic acid was heated to reflux for 1 hour. The solvent was subsequently distilled off on a rotary evaporator and the distillate was extracted twice with methylene chloride. The distillation residue (a yellow oil) was diluted with 200 ml of water, neutralized with sodium carbonate solution and extracted three times with methylene chloride. The organic phases were washed with saturated sodium carbonate solution and the aqueous phases were back-extracted with methylene chloride. The organic phases were dried over magnesium sulphate and evaporated. Distillation of the residual, yellow oil gave 6.7 g (93%) of 4-formylcyclohexanone at 70° C./0.15 Torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05013478
Source datasetuspto-grants-1991_05
ORD IDord-d7d2ba98a56c4523bcdcc6e3ebdc8ea4
Source noteuspto-grants-1991_05