HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789448Generated: October 26, 2026
Ethylene Oxide → 3-Butyn-1-ol, 4-(4-chlorophenyl)-
https://huagongshe.com/reaction/1789448
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Benzene, 1-chloro-4-ethynyl- | HCID 70118 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Butyn-1-ol, 4-(4-chlorophenyl)- | HCID 12260353 | — |
Reaction Steps
Dissolve 14.2 g (0.104 mole) of 1-chloro-4-ethynylbenzene in 35 ml dry THF and cool to -78° C. Add 49 ml butyl lithium to cold reaction mixture and allow to warm to room temperature for 2 hours. After 2 hours, cool to -78° C. and the add 5.8 ml (0.114 mole) ethylene oxide in 20 ml THF. Allow to warm to room temperature. Monitor progress of reaction with thin-layer chromatography on silica gel (methylene chloride). After 18 hours, add 150 ml saturated aqueous ammonium chloride solution and extract with 150 ml diethyl ether. Wash organic layer with 2×100 ml saturated aqueous sodium chloride solution. Dry organic layer with magnesium sulfate and then filter, and evaporate solvent to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04689341 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-bdc533e715184965bbc0536d30ee978f |
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| Source note | uspto-grants-1987_08 |
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