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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241002Generated: October 30, 2026

3-Butyn-1-OL → HCID 59305318, compound

https://huagongshe.com/reaction/2241002

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Butyn-1-OLHCID 13566—
ReactantAluminumHCID 5359268—
ReactantHCID 59790308HCID 59790308—
CatalystCopper iodideHCID 83717—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventDiethyl EtherHCID 3283—
SolventTriethylamineHCID 8471—
ProductHCID 59305318HCID 5930531882.4%

Reaction Steps

In a 0.5-2 ml Biotage conical microwave vial equipped with magnetic spin vane was dissolved 1-(3-Bromo-4-fluoro-phenyl)-2-(4-difluoromethoxy-phenyl)-ethane-1,2-dione (100 mg, 0.268 mmol) in triethylamine (1.25 mL). Copper iodide (10 mg, 0.052 mmol) and Tetrakis(triphenylphosphine) palladium (20 mg, 0.017 mmol) were added. Lastly But-3-yn-1-ol (100 mg, 1.04 mmol) was added, the vial was covered with a teflon septa, an aluminum cap was crimped in place, and the assembly was set on a Biotage Emrys microwave instrument to irradiate at 80° C. for one hour. The crude reaction was diluted with diethylether (60 mL), washed with saturated ammonium chloride (2×30 mL) and purified via column chromatography on a Yamazen W-Prep 2XY using a two-step automatic gradient elution: 100% hexanes (4 min) to 18% EtOAc (12 min), hold 4 min then to 80% EtOAc (16 min) hold 15 minutes. The resultant oil was placed under high vacuum overnight to afford 80 mgs of beige solid (82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723368B2
Source datasetuspto-grants-2010_05
ORD IDord-1ff5055e7ddc41cdbf72cb3e94923974
Source noteuspto-grants-2010_05