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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188504Generated: October 27, 2026

Hydrochloric Acid → 2-[(2,2-Dimethyl-[1,3]dioxolan-4-yl-methyl)-amino]-ethanol

https://huagongshe.com/reaction/2188504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,2-DimethoxypropaneHCID 6495—
Reactant1,4-DioxaneHCID 31275—
Reactant3-[(2-Hydroxyethyl)amino]propane-1,2-diolHCID 15034945—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTriethylamineHCID 8471—
SolventDimethylacetamideHCID 31374—
Product2-[(2,2-Dimethyl-[1,3]dioxolan-4-yl-methyl)-amino]-ethanolHCID 20553666100%

Reaction Steps

The N-(hydroxyethyl)-amino-2,3-propanediol (16.5 g, 122 mmol) was treated with a solution of HCl in dioxane (33.5 ml, 134 mmol). To this solution were added 2,2-dimethoxypropane (15.3 g, 147 mmol), DMAC (50 mL), and a catalytic amount of para-toluene sulphonic acid (0.006 mol, 1.16 g). The mixture stirred at room temperature for 24 hours. Triethylamine (1 mL) was then added, and the solvents removed by rotary evaporation. The viscous crude mixture was dissolved into triethylamine (30 mL) and ethyl acetate (500 mL) and stirred at RT for 30 min. The mixture was filtered and the collected solid washed several times with ethyl acetate. The filtrate was then evaporated on a high vacuum rotary evaporator at 40° C. to give a yellow liquid (0.122 mol, 99% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08323619B2
Source datasetuspto-grants-2012_12
ORD IDord-c5b88feed488451a88ad389579438ffc
Source noteuspto-grants-2012_12