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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-(3-Methoxypropoxy)-2,3-dimethyl-1-oxo-1lambda~5~-pyridineHCID 10013379—
Product(4-(3-Methoxypropoxy)-3-methylpyridin-2-yl)methyl acetateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998445
Source datasetuspto-grants-1999_12
ORD IDord-f3cb4e8f863847d4bfd08e36a4b0e29f
Source noteuspto-grants-1999_12