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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711998Generated: October 30, 2026

Phenylacetylene → HCID 68505193, compound

https://huagongshe.com/reaction/1711998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyleneHCID 10821—
Reactant5-(4-Methoxybenzylidene)-2,2-dimethyl-1,3-dioxane-4,6-dioneHCID 367157—
ReactantSodium AscorbateHCID 23667548—
CatalystCupric acetate monohydrateHCID 165397—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 68505193HCID 6850519327.4%

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-methoxybenzylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione (65.6 mg, 0.25 mmol). The reaction mixture was stirred vigorously at 0° C. for 64 hrs, diluted with dichloromethane (2 ml) and subjected directly to flash chromatography on silica gel (hexane/EtOAc 3:1→1:1) to give 25 mg of the pure title compound as a white solid. (yield: 27%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790882B2
Source datasetuspto-grants-2010_09
ORD IDord-e78d30db6b574780acd247bcc898d9e7
Source noteuspto-grants-2010_09