HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219049Generated: October 26, 2026
Ethylene Glycol → Ethanol, 2-((2,6-dichlorophenyl)methoxy)-
https://huagongshe.com/reaction/219049
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | 1-Bromomethyl-2,6-dichlorobenzene | HCID 30159 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethanol, 2-((2,6-dichlorophenyl)methoxy)- | HCID 13341669 | — |
Reaction Steps
Sodium methoxide (104.4 g, 1.93 mol) was added portionwise to ethylene glycol (3.74 L) under N2, keeping the temperature below 35° C. After 1-2 h, 2,6-dichlorobenzylbromide (400 g, 1.67 mol) was added and the mixture heated to 55-60° C. for 1 h. On cooling to 20° C. water (2.14 L) was added and the mixture extracted with ethyl acetate (2.14 L). The aqueous layer was separated and extracted twice with ethyl acetate (2.14 L, 1.28 L). The combined organic extracts were washed with water (2.14 L) then evaporated to dryness to afford a colourless oil (371.8 g)—LC RT=4 min. This may be chromatographed on silica (Biotage) eluting with 10% ethyl acetate in 60/80 petrol to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198483B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-9313dc4723bb431c869247e548008ccc |
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| Source note | uspto-grants-2012_06 |
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