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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170258Generated: October 29, 2026

p-Toluenesulfonic acid → HCID 53932472, compound

https://huagongshe.com/reaction/2170258

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 78137770HCID 78137770—
SolventWaterHCID 962—
ProductHCID 53932472HCID 5393247299.8%

Reaction Conditions

Temperature22.5 °C

Reaction Steps

To a 250 mL four-neck reaction flask protected from atmospheric moisture by nitrogen gas throughout the course of the reaction a solution of 14.0 g 2,6,10-trimethyl-1,1-diethoxy-3,5,9-undecatriene (2D, 0.05 mol), 100 mL tetrahydrofuran and 1.2 g of PTSA was added. After stirred until homogeneous, 22 g of water was added, and further 24 h of stirring at 20-25° C. was needed until the reaction completed according to GC. Then a solution of 2 g of NaHCO3 in 20 mL water was added for neutralization. Removal of THF by vacuum distillation, 100 mL of cyclohexane was added and then stratification. The organic layer was washed with 30 mL of water, dried over anhydrous magnesium sulfate and subsequently filtered. Removal of the volatile organic solvents by evaporation at reduced pressure afforded 10.3 g of crude 2,6,10-trimethyl-3,5,9-undecatriene-1-aldehyde of formula (12).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051254B2
Source datasetuspto-grants-2015_06
ORD IDord-04d95e230a5140da86a19205606ebd94
Source noteuspto-grants-2015_06