HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2-Dimethoxypropane → HCID 86639851, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2-Dimethoxypropane | HCID 6495 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | (2S)-2,3-Dihydroxy-N-methoxy-2,N-dimethyl-propionamide | HCID 11480618 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 86639851 | HCID 86639851 | — |
Reaction Steps
The compound prepared in Example 130(a) (12.4 g), acetone (150 mL), acetone dimethylacetal (18 mL) and p-toluenesulfonic acid monohydrate (290 mg) were stirred at room temperature for an hour. The reaction mixture was concentrated, poured into a cold aqueous solution of sodium hydrogen carbonate and extracted with a mixed solution of ethyl acetate-hexane (1:1). The obtained organic layer was washed with an aqueous saturated sodium hydrogen carbonate solution, water and brine, and dried over anhydrous magnesium sulfate. The solvent was concentrated in vacuum condition and dried to give the title compound (8.4 g) having the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07968572B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-7d9442ce4d7144f2ad036ee9c9bf288e |
| Source note | uspto-grants-2011_06 |