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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711999Generated: October 30, 2026

Phenylacetylene → HCID 68503211, compound

https://huagongshe.com/reaction/1711999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
Reactant1,3-Dioxane-4,6-dione, 5-((4-bromophenyl)methylene)-2,2-dimethyl-HCID 367161—
ReactantSodium AscorbateHCID 23667548—
CatalystCupric acetate monohydrateHCID 165397—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 68503211HCID 6850321151.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of copper (II) acetate monohydrate (10 mg, 0.050 mmol) in water (0.2 ml) was treated with sodium (L)-ascorbate (20 mg, 0.10 mmol), the mixture was stirred until the mixture was turned bright orange (3 min). Subsequently, (R,M)-3-{[4-(2-diphenylphosphanyl-7-methoxy-naphthalen-1-yl)-phthalazin-1-ylamino]-phenyl-methyl}-pentan-3-ol (1st diastereomer, 33.1 mg, 0.050 mmol) and phenylacetylene (0.275 ml, 2.5 mmol) were added, the resulting mixture was stirred for 10 min at 23° C., cooled to 0° C., stirred for 5 min and treated with 5-(4-bromobenzylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione (77.7 mg, 0.25 mmol). The reaction mixture was stirred vigorously at 0° C. for 42 hrs, diluted with dichloromethane (2 ml) and subjected directly to flash chromatography on silica gel (hexane/EtOAc 3:1→1:1) to give 53 mg of the pure title compound as a white solid. (Yield: 39%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790882B2
Source datasetuspto-grants-2010_09
ORD IDord-5ffbc9db60c54654a8d628cb97eeaf31
Source noteuspto-grants-2010_09