HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-(1-Hydroxyethyl)-1,3-thiazole-2-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-[2-(1,3-Dioxolan-2-yl)-1,3-thiazol-5-yl]ethanol | HCID 59331462 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 5-(1-Hydroxyethyl)-1,3-thiazole-2-carbaldehyde | HCID 59331383 | 39.2% |
Reaction Steps
A mixture of 1-[2-(1,3-dioxolan-2-yl)-1,3-thiazol-5-yl]ethanol (1.96 g), 1M hydrochloric acid (8 mL) and acetone (20 mL) was stirred with heating under reflux for 3 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The obtained residue was subjected to silica gel column chromatography, and the title compound (0.60 g, yield 39%) was obtained as a colorless oil from a fraction eluted with ethyl acetate-hexane (2:1, volume ratio). MS: 158 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318746B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-9469dd9105bd49e7a5be4460d109cbb3 |
| Source note | uspto-grants-2012_11 |