HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Oxide → 2-(1H-Inden-1-yl)ethan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | Indene | HCID 7219 | — |
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(1H-Inden-1-yl)ethan-1-ol | HCID 23288751 | — |
Reaction Steps
The above compound is prepared as described by Howell & Taylor, J.C.S., 1957, 3013. To butyl-lithium, prepared from lithium (20.0 g) and butyl bromide (234 g) in ether, indene (116 g., 1.0 M) is added with stirring under nitrogen at -10°. After 1 hour at -10°, ethylene oxide (88 g) in ether (300 ml) is added in 1/2 hour. After warming to 10°, 500 ml water is added cautiously and stirring is continued until there is no lithium remaining. The layers are separated and the organic layer is washed once with dilute HCl and three times with water. After drying the ether is removed and the product distilled - collecting 76 g (48%) at 125-135/0.2 mm. N.M.R. establishes the position of the double bond as 2,3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04053596 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-3432ff0f7b5742a29f67107717a7eba5 |
| Source note | uspto-grants-1977_10 |