HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hexyne-2,5-diol → 5-Hydroxy-3-hexyn-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hexyne-2,5-diol | HCID 18198 | — |
| Reactant | 5-Hydroxy-3-hexyn-2-one | HCID 10898675 | — |
| Catalyst | chromium (VI) trioxide | HCID 10219390 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 5-Hydroxy-3-hexyn-2-one | HCID 10898675 | — |
| Product | 3-Hexyne-2,5-dione | HCID 11412356 | — |
Reaction Steps
To prepare Hex-3-yne-2,5-dioxe: Chromium trioxide (100 g) in concentrated sulphuric acid (90 ml) and water (550 ml) was added with vigorous stirring over 2 hours to hex-3-yne-2,5-diol (28 g) and 5-hydroxyhex-3-yn-2-one (28 g) in acetone (400 ml) at -5° to 0°. After 1 hour, water (150 ml) was added and the solution extracted with ether. The extract was washed (aqueous NaHCO3), dried (MgSO4) and distilled to give crude hex-3-yne-2,5-dione (3-6 g), B.P. 50° (bath) at 0.15 m Hg and 5-hydroxy-hex-3-yne-2-one (B.P 50°-75° at 0.2 mm Hg) 23 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05334505 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-15927505b3de48f2a1795c594db3fd72 |
| Source note | uspto-grants-1994_08 |