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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516601Generated: October 25, 2026

1-Pentyne → Ethyl (3-(pentyne-1-yl)phenyl)acetate

https://huagongshe.com/reaction/516601

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PentyneHCID 12309—
ReactantEthyl 3-(bromophenyl)acetateHCID 11470552—
Reactant1-Butanaminium, N,N,N-tributyl-, fluoride, hydrateHCID 16211673—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
ProductEthyl (3-(pentyne-1-yl)phenyl)acetateHCID 6710018080.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of ethyl(3-bromophenyl)acetate (0.3 g, 1.24 mmol) and tetrabutylammonium fluoride hydrate (0.97 g, 3.72 mmol), was treated with PdCl2(PPh3)2(26 mg, 0.037 mmol; 3 mole %) and 1-pentyne (367 μL, 3.72 mmol) in a sealed tube. The tube was heated at 80° C. for 2 h. The mixture was treated with water, and was extracted with diethyl ether. The organic extract was dried over sodium sulfate, filtered and evaporated in vacuo to give the crude product. Purification on a Biotage™ 25 M column (silica), eluting with ethyl acetate/hexane 0:1 to 2:98, gave ethyl (3-(pentyne-1-yl)phenyl)acetate as a pale yellow oil (0.23 g, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09114118B2
Source datasetuspto-grants-2015_08
ORD IDord-dad7b912b7b14a06962d5ed784b2d14b
Source noteuspto-grants-2015_08