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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499008Generated: October 31, 2026

4-Phenyl-1-butyne → HCID 118208392, compound

https://huagongshe.com/reaction/1499008

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenyl-1-butyneHCID 123360—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
ReactantHCID 90020040HCID 90020040—
CatalystGoldHCID 23985—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 118208392HCID 11820839267%

Reaction Steps

A gold (Ag(I)) catalyst {[Au(JohnPhos)NCCH3]+SbF6—} [JohnPhos:(2-biphenyl)di-tert-butylphosphine] (11.3 mg, 0.015 mmol) was put into a reaction container, and dichloroethane (0.4 mL) was put thereinto. After stirring at room temperature for 5 minutes, ethyl hydrogen hex-1-ynylphosphonate (57.0 mg, 0.3 mmol) diluted with 0.5 mL of dichloroethane was added thereto, and finally, but-3-ynylbenzene (78 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 2-ethoxy-4-n-butyl-6-phenethyl-1,2-oxaphosphorin 2-oxide (64.4 mg, 67%) which is a title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200019B2
Source datasetuspto-grants-2015_12
ORD IDord-0d10ad6cb60c47a29e85f658b863fa2e
Source noteuspto-grants-2015_12