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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509182Generated: October 30, 2026

Phenylacetylene → HCID 57779447, compound

https://huagongshe.com/reaction/509182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
ReactantEthyl bromophenylacetateHCID 97780—
ReactantSodium AscorbateHCID 23667548—
ReactantHCID 86632440HCID 86632440—
CatalystCopper SulfateHCID 24462—
SolventWaterHCID 962—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 57779447HCID 5777944765%

Reaction Steps

To a solution of ethyl 2-bromo-2-phenylacetate 21 (1.60 g, 6.58 mmol) in sodium azide/DMSO solution (0.5 M, 13.16 mL, 6.58 mmol) which had been stirred at room temperature for 1 h was added water (10 mL), sodium ascorbate (0.130 g, 0.658 mmol), phenylacetylene (0.723 mL, 6.58 mmol) and aq. copper(II) sulfate solution (1.0 M, 1.30 mL, 1.30 mmol) (in that order). The reaction mixture was stirred for 16 h. Brine was added and extraction with ethyl acetate. The organic layer was dried over Na2SO4, filtered, and concentrated. The crude material was purified by silica gel column chromatography with gradient of ethyl acetate (0-50%) in hexane to afford compound (24) as a light yellow solid (1.31 g, 65%). LRMS: calc. 307.4, found 308.4 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096565B2
Source datasetuspto-grants-2015_08
ORD IDord-46c1157c478b41429391923266b8c5aa
Source noteuspto-grants-2015_08