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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475545Generated: October 25, 2026

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

https://huagongshe.com/reaction/475545

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™ 25M 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 numberUS08637574B2
Source datasetuspto-grants-2014_01
ORD IDord-0de08e7b90404ea7ae14f2aa9466c317
Source noteuspto-grants-2014_01