HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetovanillone → 1-(3-Methoxy-4-((6-methoxypyridin-3-yl)methoxy)phenyl)ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetovanillone | HCID 2214 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-(Chloromethyl)-2-methoxypyridine hydrochloride | HCID 53438957 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(3-Methoxy-4-((6-methoxypyridin-3-yl)methoxy)phenyl)ethan-1-one | HCID 118114091 | 85% |
Reaction Steps
To a stirred suspension of 1-(4-hydroxy-3-methoxyphenyl)ethan-1-one (3.96 g, 23.82 mmol) and potassium carbonate (13.17 g, 95.29 mmol) in acetonitrile (75 mL) was added 5-(chloromethyl)-2-methoxypyridine hydrochloride (4.85 g, 25.01 mmol). After 2 h, the mixture was diluted with water (150 mL) and extracted with dichloromethane (3×100 mL). The combined organic phases were dried over magnesium sulfate, filtered, and concentrated to provide a yellow oil. Trituration of the crude material with hexanes afforded 5.48 g (85%) of 1-(3-methoxy-4-((6-methoxypyridin-3-yl)methoxy)phenyl)ethan-1-one as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09067914B1 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-101b6d74a5a14d1e8fba35a0fc0d54be |
| Source note | uspto-grants-2015_06 |