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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537598Generated: October 25, 2026

Hydrochloric Acid → 2-Docosyloxy-4-methoxybenzyl alcohol

https://huagongshe.com/reaction/537598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Hydroxy-4-MethoxybenzaldehydeHCID 69600—
Reactant1-BromodocosaneHCID 81355—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
Product2-Docosyloxy-4-methoxybenzyl alcoholHCID 5325721064.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

2-Hydroxy-4-methoxybenzaldehyde (5 g, 32.9 mmol), 1-bromodocosane (16.6 g, 42.7 mmol) and potassium carbonate (14.8 g, 107 mmol) were mixed with DMF (150 ml), and the mixture was stirred at 100° C. for 7 hr. Chloroform (400 ml) and 1N hydrochloric acid (300 ml) were added to the reaction mixture, and the mixture was washed. The organic layer was washed successively with 1N hydrochloric acid and saturated brine. The organic layer was concentrated and slurry-washed with methanol. The precipitate was collected by filtration and dried under reduced pressure. The obtained dried crystals were dissolved in THF (150 ml), sodium borohydride (3.7 g) was added, and the mixture was stirred at 40° C. for 3 hr. 1N Hydrochloric acid was added to the reaction mixture, and the mixture was concentrated. The mixture was extracted with chloroform, and washed successively with aqueous sodium hydrogen carbonate solution and saturated brine. The organic layer was concentrated. The obtained residue was washed with acetonitrile, and the precipitate was collected by filtration and dried under reduced pressure to give 2-docosyloxy-4-methoxybenzyl alcohol (9.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859732B2
Source datasetuspto-grants-2014_10
ORD IDord-1e8858f487b24899b0dcdb987cbceddc
Source noteuspto-grants-2014_10