HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374522Generated: October 30, 2026
Benzyl Chloride → Hexaethylene Glycol Monobenzyl Ether
https://huagongshe.com/reaction/1374522
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hexaethylene Glycol | HCID 17472 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | Hexaethylene Glycol Monobenzyl Ether | HCID 11164646 | 70.6% |
Reaction Steps
An aqueous sodium hydroxide solution prepared by dissolving 3.99 g (100 mmol) NaOH in 4 ml water was added slowly to monodispersed hexaethylene glycol (28.175 g, 25 ml, 100 mmol). Benzyl chloride (3.9 g, 30.8 mmol, 3.54 ml) was added and the reaction mixture was heated with stirring to 100° C. for 18 hours. The reaction mixture was then cooled, diluted with brine (250 ml) and extracted with methylene chloride (200 ml×2). The combined organic layers were washed with brine once, dried over Na2SO4, filtered and concentrated in vacuo to a dark brown oil. The crude product mixture was purified via flash chromatography (silica gel, gradient elution: ethyl acetate to 9/1 ethyl acetate/methanol) to yield 8.099 g (70%) of monodispersed compound 1 as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07166571B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-516e073a0db541218ca8bc0740e14034 |
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| Source note | uspto-grants-2007_01 |
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