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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248021Generated: October 27, 2026

Acetic Anhydride → HCID 19016453, compound

https://huagongshe.com/reaction/248021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(Tetradecyloxy)benzenemethanamineHCID 11723498—
SolventDichloromethaneHCID 6344—
ProductHCID 19016453HCID 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 numberUS05208247
Source datasetuspto-grants-1993_05
ORD IDord-c1ce92ccf637497182e47cb7677d66e9
Source noteuspto-grants-1993_05