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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458481Generated: October 25, 2026

Water → 3,5-Bis(10-hydroxydecyloxyl)benzaldehyde

https://huagongshe.com/reaction/458481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-DihydroxybenzaldehydeHCID 94365—
Reactant1-Decanol, 10-bromo-HCID 104507—
SolventDimethylformamideHCID 6228—
Product3,5-Bis(10-hydroxydecyloxyl)benzaldehydeHCID 58820701—

Reaction Conditions

Temperature50 °C

Reaction Steps

1.18 g of 3,5-dihydroxybenzaldehyde A-2 (8.56 mmol) and 6.15 g of K2CO3 (44.5 mmol, 5.2 eq.) were added to 4.47 g of 10-bromodecane-1-ol A-1 (18.8 mmol, 2.2 eq.) dissolved in 100 mL of DMF, and the mixture was stirred in nitrogen atmosphere at 50° C. for 48 hours. After the temperature was returned to room temperature, the reaction was stopped by adding 50 mL of water and the organic layer was extracted with ether (100 mL×3). The extracted organic layers were combined, washed with saturated brine and dried with anhydrous Na2SO4. The solvent was removed by using an evaporator, whereby brown liquid A-3 was obtained (crude yield: 4.418 g). The product was not purified at this stage and directly used for the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192650B2
Source datasetuspto-grants-2007_03
ORD IDord-07b28ce665fb4c639f8a601b30a280bc
Source noteuspto-grants-2007_03