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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711996Generated: October 31, 2026

Phenylacetylene → HCID 12173663, compound

https://huagongshe.com/reaction/1711996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
Reactant5-Benzylidene-2,2-dimethyl-1,3-dioxane-4,6-dioneHCID 599888—
ReactantSodium AscorbateHCID 23667548—
CatalystCupric acetate monohydrateHCID 165397—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 12173663HCID 1217366365.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of copper (II) acetate monohydrate (20 mg, 0.10 mmol) in water (0.4 ml) was treated with sodium (L)-ascorbate (40 mg, 0.20 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, 66.2 mg, 0.10 mmol) and phenylacetylene (0.55 ml, 5.0 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-benzylidene-2,2-dimethyl-1,3-dioxane-4,6-dione (116 mg, 0.50 mmol). The reaction mixture was stirred vigorously at 0° C. for 66 hrs, diluted with dichloromethane (2 ml) and subjected directly to flash chromatography on silica gel (hexane/EtOAc 3:1→1:1) to give 110 mg of the pure title compound as a white solid. (yield: 64%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790882B2
Source datasetuspto-grants-2010_09
ORD IDord-42e0caafc70a4aaab3e21fddb7c68460
Source noteuspto-grants-2010_09