HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-methoxypyridin-2-yl)methyl Acetate → (4-Methoxy-pyridin-2-yl)-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-methoxypyridin-2-yl)methyl Acetate | HCID 10726082 | — |
| Catalyst | Mercury | HCID 23931 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | (4-Methoxy-pyridin-2-yl)-methanol | HCID 10820596 | 67% |
Reaction Steps
A solution of 2-acetoxymethyl-4-methoxypyridine (20.72 g, 0.114 mole) in 3M hydrochloric acid (100 ml) was heated under reflux for 1 hour. The resulting solution was concentrated under reduced pressure and the residue neutralised by addition of potassium carbonate. The mixture was extracted with dichloromethane and the organic solution dried over anhydrous sodium sulphate, filtered and evaporated to give a light coloured viscous oil which solidified on standing to yield the title compound (10.6 g, 67%) b.p. 135° C. at 0.1 mm mercury.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04562197 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-d43c60e54378460d8ad0d58a360d0b13 |
| Source note | uspto-grants-1985_12 |