HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414077Generated: November 2, 2026
1-Bromo-2-Chloroethane → HCID 86741981, compound
https://huagongshe.com/reaction/2414077
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-2-Chloroethane | HCID 7849 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | 2-Propylvaleronitrile | HCID 83330 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 86741981 | HCID 86741981 | — |
Reaction Steps
To the solution (245 ml) of 1,6M n butyllithium in hexane is added, drop by drop in an atmosphere of nitrogen and with stirring, the solution of 28.8 g of diethylamine in 100 ml of anhydrous ether. After 1 hour, the solution of 49.2 g of 2-propyl pentane nitrile in 100 ml of anhydrous ether is added at ambient temperature then, after return to ambient temperature, the solution of 49.1 g of 1-bromo 2-chloro ethane in 700 ml of anhydrous ether is added. The mixture is taken to reflux for 15 hours then, whilst cooling the reaction mixture in an ice bath, water is added. The organic phase is separated, washed with water, then with a dilute solution of hydrochloric acid and again with water. It is dried over sodium sulfate and the solvent is evaporated. The residue is distilled and a liquid is obtained; b.p./20 mm Hg: 140°-150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04721710 |
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| Source dataset | uspto-grants-1988_01 |
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| ORD ID | ord-c1dc846746ee4ceabfa96141e679cd84 |
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| Source note | uspto-grants-1988_01 |
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