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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257541Generated: October 31, 2026

Acetic Anhydride → 1-(3-Methylphenyl)-2-[2-(morpholin-4-yl)ethoxy]ethyl acetate

https://huagongshe.com/reaction/2257541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 53902928HCID 53902928—
SolventPyridineHCID 1049—
Product1-(3-Methylphenyl)-2-[2-(morpholin-4-yl)ethoxy]ethyl acetateHCID 3076618—

Reaction Steps

0.65 ml of pyridine and 0.99 ml of acetic anhydride were added to 1 g of 1-(3-methylphenyl)-2-[2-(morpholin-4-yl)ethoxy]ethanol. The mixture was stirred for 3 hours at room temperature. The reaction mixture was subjected to distillation under reduced pressure to remove the solvent. To the residue were added 20 ml of ethyl acetate and 10 ml of water. The mixture was adjusted to pH 10 with potassium carbonate. The organic layer was separated, washed with water and a saturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography (eluant:chloroform/ethanol=30/1) to obtain 1 g of oily 1-acetoxy-1-(3-methylphenyl)-2-[2-(morpholin-4-yl)ethoxy]ethane (compound No. 178).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05658904
Source datasetuspto-grants-1997_08
ORD IDord-3e045298f03e4da58d4fc050fb34e0ae
Source noteuspto-grants-1997_08