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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225706Generated: October 31, 2026

Triethylene Glycol → HCID 53897125, compound

https://huagongshe.com/reaction/2225706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylene GlycolHCID 8172—
ReactantHCID 19004267HCID 19004267—
SolventDichloromethaneHCID 6344—
ProductHCID 53897125HCID 53897125—

Reaction Steps

The acid chloride, prepared from 4-[[2-(2-naphthalenyloxy)ethyl]oxy]-alpha-oxobenzene-acetic acid (0.5 g) as described in Example 6, was dissolved in dichloromethane (10 mL) and added dropwise to a stirred, cold (<-50° C.) mixture of triethylene glycol (0.9 g) in dichloro-methane (10 mL). The cooling bath was removed and the mixture stirred for 1 hour at room temperature. The mixture was diluted with dichloromethane and washed once with saturated aqueous sodium bicarbonate, once with water, and the organic solution was dried (Na2SO4), filtered, and evaporated to give crude product. The material was purified by HPLC (dichloro-methane-ethyl acetate; 2:1) to provide, after crystallization from ethyl acetate-hexane, 0.36 g of 4-[[2-(2-naphthalenyloxy)ethyl]oxy]-alpha-oxobenzeneacetic acid 2-[2-(2-hydroxyethoxy)ethoxy]ethyl ester as a colorless solid, mp 70°-71° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344843
Source datasetuspto-grants-1994_09
ORD IDord-093eea8ce8564cf3ada812be7e90d553
Source noteuspto-grants-1994_09