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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728886Generated: November 2, 2026

Acetic Anhydride → N-[[4-(Tetradecyloxy)phenyl]methyl]acetamide

https://huagongshe.com/reaction/1728886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(Tetradecyloxy)benzenemethanamineHCID 11723498—
SolventDichloromethaneHCID 6344—
ProductN-[[4-(Tetradecyloxy)phenyl]methyl]acetamideHCID 19016453—

Reaction Steps

To a room temperature mixture of 15 g of product from Example 99, 0.229 g of 4-N,N-dimethylaminopyridine and 50 ml of methylene chloride is added 5 ml of acetic anhydride. An additional 50 ml of methylene chloride is added and the solution is stirred at room temperature for 69 hours. The reaction is poured into half saturated sodium bicarbonate and extracted with methylene chloride. The combined organic layers are washed with half saturated sodium bicarbonate, water and saturated sodium chloride. The dried methylene chloride layer is concentrated in vacuo and purified by chromatography (silica gel: 5% methyl alcohol/chloroform) to give 16.29 g of the desired product as colorless prisms.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05328921
Source datasetuspto-grants-1994_07
ORD IDord-ecfe7556d2cf4a0baf413b373b75f073
Source noteuspto-grants-1994_07