HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499001Generated: November 3, 2026
Triethylamine → Ethyl 5-chloropent-1-en-2-yl p-tolylethynylphosphonate
https://huagongshe.com/reaction/1499001
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Pentyne, 5-chloro- | HCID 84308 | — |
| Reactant | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | — |
| Reactant | Ethyl hydrogen p-tolylethynylphosphonate | HCID 71546601 | — |
| Catalyst | Gold | HCID 23985 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | Ethyl 5-chloropent-1-en-2-yl p-tolylethynylphosphonate | HCID 90019180 | 70% |
Reaction Steps
A gold (Ag(I)) catalyst {[Au(JohnPhos)NCCH3]+SbF6—} [JohnPhos:(2-biphenyl)di-tert-butylphosphine] (11.3 mg, 0.015 mmol) and triethylamine (Et3N) (3.0 mg, 0.03 mmol) were put into a reaction container, and dichloroethane (0.4 mL) was put thereinto. After stirring at room temperature for 5 minutes, ethyl hydrogen p-tolylethynylphosphonate (67.3 mg, 0.3 mmol) diluted with 0.5 mL of dichloroethane was added thereto, and finally, 5-chloropent-1-yne (61.5 mg, 0.6 mmol) was put thereinto. Then, when all of the starting materials disappeared in the TLC, the reaction was allowed to be completed. After the solvent was removed under low atmospheric pressure, the product was separated by chromatography to obtain ethyl 5-chloropent-1-en-2-yl p-tolylethynylphosphonate (68.5 mg, 70%) which is a title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09200019B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-14c9c66d7c7a49eb944b9d8da3dfddeb |
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| Source note | uspto-grants-2015_12 |
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