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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973902Generated: October 31, 2026

Acetic Anhydride → HCID 13154060, compound

https://huagongshe.com/reaction/1973902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 13154059HCID 13154059—
SolventTolueneHCID 1140—
ProductHCID 13154060HCID 13154060—

Reaction Steps

20.4 g (0.2 mol) of acetic anhydride are added dropwise to a solution of 19.5 g (0.1 mol) of 4-methoxy-5-n-butyl-2-picoline-N-oxide in 100 ml of toluene over the course of 15 minutes, whilst stirring. Thereafter the mixture is heated for 8 hours under reflux. After evaporation to dryness in vacuo, the mixture is rendered alkaline with 2 N aqueous sodium carbonate solution and is extracted with ether. The ether phases are combined, dried with sodium sulphate, filtered and evaporated. Distillation of the residue in a bulb tube in a high vacuum at 120° yields 2-acetoxymethyl-4-methoxy-5-n-butyl-pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03998955
Source datasetuspto-grants-1976_12
ORD IDord-e874a6d5719e4183a7c44ac338061d01
Source noteuspto-grants-1976_12