HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6636Generated: October 25, 2026
Diethylene Glycol Monomethyl Ether → Ethyl 2,5,8,11,14,17,20,23-octaoxanonacosan-29-oate
https://huagongshe.com/reaction/6636
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethylene Glycol Monomethyl Ether | HCID 8134 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-{2-[2-(2-{2-[2-(2-Methylsulfonylethoxy) ethoxy]ethoxy}-ethoxy)-ethoxy]-ethoxy}-hexanoic acid ethyl ester | HCID 86587027 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 2,5,8,11,14,17,20,23-octaoxanonacosan-29-oate | HCID 71366717 | 62.6% |
Reaction Steps
NaH (88 mg of a 60% dispersion in oil, 2.2 mmol) was suspended in anhydrous toluene (3 ml) under N2 and chilled to 0° C. Non-polydispersed diethylene glycol monomethyl ether (0.26 ml, 0.26 g, 2.2 mmol) that had been dried via azeotropic distillation with toluene was added. The reaction mixture was allowed to warm to room temperature and stirred for four hours, during which time the cloudy grey suspension became clear and yellow and then turned brown. Mesylate 20 (0.50 g, 1.0 mmol) in 2.5 ml dry toluene was added. After stirring at room temperature over night, the reaction was quenched by the addition of 2 ml of methanol and the resultant solution was filtered through silica gel. The filtrate was concentrated in vacuo and the FAB MS: m/e 499 (M+H), 521 (M+Na). Additional purification by preparatory chromatography (silica gel, 19/3 chloroform/methanol) provided the non-polydispersed product as a clear yellow oil (0.302 g 57%). FAB MS: m/e 527 (M+H), 549 (M+Na).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07084121B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-b91745a89bd4417cb01af8e321354d1d |
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| Source note | uspto-grants-2006_08 |
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