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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Pentyne, 5-chloro-HCID 84308—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
ReactantEthyl hydrogen p-tolylethynylphosphonateHCID 71546601—
CatalystGoldHCID 23985—
Solvent1,1-DichloroethaneHCID 6365—
ProductEthyl 5-chloropent-1-en-2-yl p-tolylethynylphosphonateHCID 9001918070%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200019B2
Source datasetuspto-grants-2015_12
ORD IDord-14c9c66d7c7a49eb944b9d8da3dfddeb
Source noteuspto-grants-2015_12