HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6502Generated: October 28, 2026
1,2-Dichloroethane → 1-(4-Ethoxyphenyl)cyclopropanecarbonitrile
https://huagongshe.com/reaction/6502
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-(4-Ethoxyphenyl)acetonitrile | HCID 583905 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1-(4-Ethoxyphenyl)cyclopropanecarbonitrile | HCID 13537251 | — |
Reaction Steps
To 7.5 ml (0.012 mol) of 1.7M n-butyllithium in hexane, at room temperature, under an atmosphere of nitrogen, is added rapidly 10 ml of anhydrous tetrahydrofuran, followed by a solution of 4-ethoxyphenyl acetonitrile (0.8 g 0.005 mol) in 4 ml of tetrahydrofuran, during 5 minutes. The reaction mixture is stirred magnetically for 1 hour then treated with 0.50 g (0.005 mol) of 1,2-dichloroethane in 10 ml of tetrahydrofuran, during a period of 40 minutes (slow addition is important). After 16 hours, the mixture is hydrolysed by 10 ml of 3N HCl and then taken up in ether, washed with water, sodium bicarbonate, water and dried over anhydrous sodium sulphate. The solvent is removed under reduced pressure. Yield: 0.64 g of a viscous semi-crystalline oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05248834 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-4fe44030a62b460f8a5604dcd68ea078 |
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| Source note | uspto-grants-1993_09 |
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