HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → 1-(5-Hydroxy-2-neopentylpyridin-4-yl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-(5-(Methoxymethoxy)-2-neopentylpyridin-4-yl)ethanone | HCID 57515876 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 1-(5-Hydroxy-2-neopentylpyridin-4-yl)ethanone | HCID 57515877 | — |
Reaction Steps
A solution of 1-(5-(methoxymethoxy)-2-neopentylpyridin-4-yl)ethanone (21.6 g, 86 mmol) in (2:1:1) 5 M HCl: i-PrOH : THF (800 mL) was stirred 4 h at rt. The mixture was concentrated to remove the THF and i-PrOH. The resulting solution consisting of the product in aqueous HCl was quenched by slow addition to a solution of saturated aqueous NaHCO3 (500 mL) containing excess solid NaHCO3 (50 g). The aqueous layer was extracted with CH2Cl2 (3×250 mL), the organic layers combined and washed with saturated aqueous NaCl (250 mL), dried (MgSO4), and concentrated to give 1-(5-hydroxy-2-neopentylpyridin-4-yl)ethanone as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745484B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-7537d8293d6048abad04b7051b233686 |
| Source note | uspto-grants-2010_06 |