HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 609838Generated: October 31, 2026
Acetic Anhydride → (4-(3-Methoxypropoxy)-3-methylpyridin-2-yl)methyl acetate
https://huagongshe.com/reaction/609838
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-(3-Methoxypropoxy)-2,3-dimethyl-1-oxo-1lambda~5~-pyridine | HCID 10013379 | — |
| Product | (4-(3-Methoxypropoxy)-3-methylpyridin-2-yl)methyl acetate | HCID 19600546 | — |
Reaction Steps
20 ml of acetic anhydride was added to 760 mg (3.6 mmol) of 4-(3-methoxypropoxy)-2,3-dimethyl-pyridine N-oxide to carry out the reaction at 90° C. for one hour. The reaction mixture was distilled to remove the acetic anhydride, followed by the addition of a saturated aqueous solution of sodium hydrogen-carbonate. The obtained mixture was extracted with chloroform. The extract was concentrated to obtain 700 mg of 2-acetoxymethyl-4-(3-methoxypropoxy)-3-methylpyridine as a brown oil. 500 mg of sodium hydroxide and 15 cc of ethanol were added to the 2-acetoxymethyl-4-(3-methoxypropoxy)-3-methylpyridine prepared above. The obtained mixture was stirred at 50° C. for one hour. After the completion of the reaction, the reaction mixture was distilled to remove the ethanol, followed by the addition of water. The obtained mixture was extracted with chloroform. The obtained chloroform layer was concentrated to obtain 450 mg of 2-hydroxymethyl-4-(3-methoxypropoxy)-3-methylpyridine as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05998445 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-f3cb4e8f863847d4bfd08e36a4b0e29f |
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| Source note | uspto-grants-1999_12 |
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