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HRID 59021作成日:2026年10月25日

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

https://huagongshe.com/reaction/59021

反応式

関与物質

役割名称HCID仕込み量
反応物1-PentyneHCID 12309—
反応物Ethyl 3-(bromophenyl)acetateHCID 11470552—
反応物1-Butanaminium, N,N,N-tributyl-, fluoride, hydrateHCID 16211673—
触媒HCID 178418476HCID 178418476—
溶媒WaterHCID 962—
生成物Ethyl (3-(pentyne-1-yl)phenyl)acetateHCID 6710018080.5%

反応条件

温度80 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09439882B2
出典データセットuspto-grants-2016_09
ORD IDord-88dbc1b4edb54ade9774a49832ce807e
出典メモuspto-grants-2016_09