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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716498Generated: October 30, 2026

Water → HCID 86687811, compound

https://huagongshe.com/reaction/716498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium HypochloriteHCID 23665760—
ReactantHCID 66584098HCID 66584098—
CatalystPotassium BromideHCID 253877—
CatalystTempoHCID 2724126—
SolventTolueneHCID 1140—
ProductHCID 86687811HCID 8668781145%

Reaction Conditions

Temperature0 °C

Reaction Steps

KBr (0.6 g, 0.005 mol) and NaHCO3 (6.4 g, 0.076 mol) and 0.8 g (0.00566 mols) 2,2,6,6-Tetramethylpiperidine-1-oxyl (TEMPO) were mixed together with water (60 ml), toluene (250 g) and 3-Methyl-4(3,3,5-trimethylcyclohex-1-yl) butan-1-ol (96 g 0.45 mol, purity: 98% sum of the isomers) the reaction temperature maintain 0° C. with continuous stirring. NaOCl (13% w/w aqueous 426.8 g, 0.745 mol) was added to the reaction mass over 2 h. Stirring was continued for another 12 h. The aqueous phase was removed, organic phase was washed with a solution of NaHCO3 and then with water. The organic phase thus obtained was concentrated and crude product purified by fractional distillation to provide 3-Methyl-4(3,3,5-trimethylcyclohexyl) butanal (42.63 g, yield: 45%, GC purity: 96% sum of isomers).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187709B2
Source datasetuspto-grants-2015_11
ORD IDord-0326ae35458d4bcabe40252aae5453bb
Source noteuspto-grants-2015_11