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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254952Generated: October 31, 2026

Water → 4-Oxocyclohexane-1-carbaldehyde

https://huagongshe.com/reaction/2254952

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, at 70° C./0.15 Torr, 6.7 g (93%) of 4-formylcyclohexanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05238602
Source datasetuspto-grants-1993_08
ORD IDord-c237b2368f684628bd54010c7536790c
Source noteuspto-grants-1993_08