HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 2-(3-(2-Methylphenyl)-3-phenyl-2-propen-1-yloxy)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | HCID 54536217 | HCID 54536217 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(3-(2-Methylphenyl)-3-phenyl-2-propen-1-yloxy)ethanol | HCID 53952760 | 45% |
Reaction Steps
A solution of n-butyllithium in hexanes (13.0 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 0.5 h at room temperature. 3-Bromo-1-(2-methylphenyl)-1-phenyl-1-propene (9.3 g, 32 mmol) was added and the reaction mixture was stirred at room temperature for 100 h. The mixture was poured into water (200 ml) and extracted with ethyl acetate (3×75 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 THF (4:1) as eluent provided 3.9 g (45%) of 2-(3-(2-methyl-phenyl)-3-phenyl-2-propen-1-yloxy)ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06174898B1 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-1e6f8fd90895457a869e2c88261f8d72 |
| Source note | uspto-grants-2001_01 |