HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225706Generated: October 31, 2026
Triethylene Glycol → HCID 53897125, compound
https://huagongshe.com/reaction/2225706
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylene Glycol | HCID 8172 | — |
| Reactant | HCID 19004267 | HCID 19004267 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53897125 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05344843 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-093eea8ce8564cf3ada812be7e90d553 |
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| Source note | uspto-grants-1994_09 |
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