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HRID 561997作成日:2026年10月24日

Acetaldehyde → 1-(2,6-Difluoro-4-iodophenyl)ethanol

https://huagongshe.com/ja/reaction/561997

反応式

関与物質

役割名称HCID仕込み量
反応物AcetaldehydeHCID 177—
反応物1,3-Difluoro-5-iodobenzeneHCID 2778221—
反応物1,2,2,3-TetramethylpiperidineHCID 18761772—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1-(2,6-Difluoro-4-iodophenyl)ethanolHCID 6700129947.4%

反応手順

To a solution of 2.5 M n-butyl lithium in hexanes (2 mL, 5.0 mmol) and tetrahydrofuran (20 mL) at −78° C. under an atmosphere of nitrogen was added dropwise tetramethylpiperidine (0.85 mL, 5.0 mmol). The resulting light yellow solution was stirred for approximately 15 minutes, then 1,3-difluoro-5-iodo-benzene (1 g, 4.17 mmol) was added dropwise. This solution was stirred at −78° C. for 1 hour, followed by the addition of acetaldehyde (0.70 mL, 12.5 mmol) via syringe. The reaction mixture was stirred at −78° C. for 10 minutes then allowed to warm to room temperature. TLC indicated the reaction to be complete. The reaction was quenched with saturated aqueous ammonium chloride solution (2 mL), diluted with water (50 mL) and extracted with ethyl acetate (2×30 mL). The combined organic layers were dried over sodium sulfate and concentrated in vacuo. The crude product was purified by chromatography over silica gel gradient eluted with 0 to 25% v/v ethyl acetate/hexanes to give 1-(2,6-difluoro-4-iodo-phenyl)-ethanol (561 mg, 47%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063085B2
出典データセットuspto-grants-2011_11
ORD IDord-4732835dd49a442cbe2e7f06b3806d3e
出典メモuspto-grants-2011_11