Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Ethynylthiophene | HCID 5246258 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | Ethanone, 2-chloro-1-(1-chlorocyclopropyl)- | HCID 11062580 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 131717191 | HCID 131717191 | 97.3% |
Reaction Steps
22.2 g (0.203 mole) of ethyl bromide are slowly added to 4.9 g (0.203 mole) of magnesium turnings in 100 ml of diethyl ether. After completion of the addition, the reaction mixture is heated under reflux for 30 minutes and then cooled to room temperature, and a solution of 20 g (0.185 mole) of 2-thienylethine in 50 ml of diethyl ether is subsequently added dropwise with stirring. The mixture is heated under reflux for 1 hour and again cooled to room temperature. 28.3 g (0.185 mole) of 1-chloro-cyclopropyl chloromethyl ketone are added dropwise with stirring and the mixture is then heated under reflux for a further 2 hours. After cooling to room temperature, the reaction mixture is poured into a saturated aqueous ammonium chloride solution and the mixture is extracted three times with diethyl ether. The combined organic phases are washed once with water, dried over sodium sulphate and concentrated under reduced pressure. 47.0 g (97% of theory) of 1-chloro-2-(1-chloro-cyclopropyl)-4-(thiophen-2-yl)-but-3-in-2-ol are obtained in this way in the form of an oil which is reacted further without additional purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05096912 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-a8c57d338b6c45b795d6aebe1c07ca73 |
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| Source note | uspto-grants-1992_03 |
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