HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967360Generated: October 31, 2026
Carbon Dioxide → HCID 178528060, compound
https://huagongshe.com/reaction/967360
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | Zincchloride | HCID 3007855 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 178528060 | HCID 178528060 | — |
Reaction Steps
The flask was charged with 120 mg (1.1 mmol) of phenylacetylene and 4 mL of tetrahydrofuran, and the flask was cooled to −78° C. in a cooling bath with ethanol and dry ice. Thereafter, 0.65 mL (1.0 mmol) of a 1.56 mol/L hexane solution of n-butyllithium was slowly added over a period of 20 minutes. After stirring the mixture at −78° C. for 30 minutes, a suspension of 140 mg (1.0 mmol) of zinc chloride in 1 mL of tetrahydrofuran was added thereto. The mixture was stirred at −78° C. for additional 1 hour, thereafter the cooling bath was removed, and the mixture was allowed to stand upto room temperature. The resulting solution was used as (phenylethynyl)zinc reagent [(Ph—C≡C—ZnCl].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06953871B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-f9de1321844a4345a79ad6d8abab17ea |
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| Source note | uspto-grants-2005_10 |
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