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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424743Generated: October 25, 2026

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

https://huagongshe.com/reaction/1424743

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 (367 372 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 numberUS08927765B2
Source datasetuspto-grants-2015_01
ORD IDord-ab38326c267a437191510fa68a12f04e
Source noteuspto-grants-2015_01