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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045111Generated: October 31, 2026

Phenylacetylene → HCID 58387189, compound

https://huagongshe.com/reaction/1045111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
ReactantEthylacetate methanolHCID 21584119—
ReactantHCID 59267806HCID 59267806—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
ProductHCID 58387189HCID 58387189—

Reaction Steps

A 4 mL vial equipped with a stirring bar was charged with copper iodide (2.0 mg, 10 mol %), and Pd(PPh3)2Cl2 (3.5 mg, 5 mol %). A solution of 6-chloro-5-iodo-2-methanesulfonyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-benzoimidazole (Intermediate 5, 49.0 mg, 0.100 mmol) in DMF (0.5 mL) was added to the vial, followed by a solution of ethynyl-benzene (20.0 mg, 0.200 mmol) in DMF (0.5 mL) and TEA (98 uL, 0.70 mmol). The resulting suspension was stirred at rt for 10 min, during which time it gradually turned brown. The solvent was then removed in vacuo to give brown oily solid, which was suspended in 1:1 EtOAc/MeOH (3 mL) and passed through a Thiol StratoSphere™ SPE cartridge (Polymer Labs). The resulting solution was evaporated to dryness in vacuo to give light yellow oil. LR-MS (API-ES): calculated C22H25ClN2O3SSi 460.1, m/e (M+H)+ not observed, 433.0, 403 (Rt 3.83 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563746B2
Source datasetuspto-grants-2013_10
ORD IDord-62dbfb4403b744349bdafda000f8a832
Source noteuspto-grants-2013_10