HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → (5-amino-2,2-dimethyl-1,3-dioxan-5-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2,2-Dimethoxypropane | HCID 6495 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tromethamine hydrochloride | HCID 93573 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (5-amino-2,2-dimethyl-1,3-dioxan-5-yl)methanol | HCID 300060 | 85% |
Reaction Steps
Tris hydrochloride (51 g, 324 mmol) was suspended in dry DMF (100 ml) and 2,2-dimethoxypropane (39 g, 374 mmol) was added followed by para-toluenesulfonic acid (2.6 g, 13.5 mmol). The mixture was stirred in a sealed flask for 18 h at ambient temperature when a clear solution resulted. Triethylamine (2.5 ml) was added and solvent evaporated. The viscous crude was dissolved in triethylamine (40 ml) and ethyl acetate (750 ml) added and the white precipitate of ammonium salts was filtered off after stirring for 30 mins. The filtrate was evaporated to give the product as a colourless liquid in approx. 85% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08202511B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-835eca6df61749bda7b4d45190b4ebd3 |
| Source note | uspto-grants-2012_06 |