HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566556Generated: October 30, 2026
Ethylene Glycol → HCID 10782137, compound
https://huagongshe.com/reaction/566556
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | HCID 21266348 | HCID 21266348 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 10782137 | HCID 10782137 | 66% |
Reaction Steps
A solution of n-butyllithium in hexanes (15.0 ml, 2.5 M) was added dropwise under a nitrogen atmosphere to ethylene glycol (30 ml) at 10° C. When addition was complete the mixture was stirred for 0.5 h at room temperature. 3-Bromo-1,1-bis(4-chlorophenyl)-1-propene (13.0 g, 38 mmol, prepared similarly to the method described in Example 26) was added and the reaction mixture was stirred at room temperature for 72 h. The mixture was poured into water (100 ml) and extracted with ethyl acetate (2×75 ml). The combined organic extracts was dried (Na2SO4) and the solvent evaporated in vacuo. Flash chromatography of the residue on silica gel (200 g) using a mixture of n-heptane and ethyl acetate (3:2) as eluent provided 8.1 g (66%) of 2-(3,3-bis-(4-chlorophenyl)-2-propen-1-yloxy)ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06174898B1 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-c54ba29474784e5ca0499dcf738ac1c6 |
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| Source note | uspto-grants-2001_01 |
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