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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,2-Dimethoxypropane | HCID 6495 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 3-[(2-Hydroxyethyl)amino]propane-1,2-diol | HCID 15034945 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 2-[(2,2-Dimethyl-[1,3]dioxolan-4-yl-methyl)-amino]-ethanol | HCID 20553666 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08323619B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-c5b88feed488451a88ad389579438ffc |
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| Source note | uspto-grants-2012_12 |
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