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HRID 70294作成日:2026年10月24日

1-Bromo-3-ethynylbenzene → [4-(3-bromophenyl)-1H-1,2,3-triazol-1-yl]methyl 2,2-dimethylpropanoate

https://huagongshe.com/ja/reaction/70294

反応式

関与物質

役割名称HCID仕込み量
反応物1-Bromo-3-ethynylbenzeneHCID 11480818—
反応物Azidomethyl 2,2-dimethylpropanoateHCID 11521126—
反応物Sodium AscorbateHCID 23667548—
溶媒WaterHCID 962—
溶媒2-Methylpropan-2-ol--water (1/1)HCID 71401949—
生成物[4-(3-bromophenyl)-1H-1,2,3-triazol-1-yl]methyl 2,2-dimethylpropanoateHCID 58276391—

反応手順

To a mixture of 1-bromo-3-ethynylbenzene (0.430 g; 2.38 mmol; Note 1), and azidomethyl 2,2-dimethylpropanoate (0.391 g; 2.49 mmol; Note 2) in t-BuOH/water (3.5/3.0 mL respectively) at room temperature was added a solution of CuSO4.5H2O in water (0.030 g/0.5 mL), followed by sodium ascorbate (0.141 g; 0.71 mmol) in one portion. The mixture was stirred 25 h at room temperature, diluted with water and extracted with EtOAc (×3). Combined organics were washed (5% NH4OH, water, brine), dried over Na2SO4 and concentrated in vacuo affording the title compound as a tan solid which was used without further purification. LC/MS (method B) 2.77 min, m/z 338, 340 (M+H, Br isotopes).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822518B2
出典データセットuspto-grants-2014_09
ORD IDord-7bf576b506234e78b7e26709df696d9d
出典メモuspto-grants-2014_09