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HRID 1241478作成日:2026年10月27日

4-Chloro-3-Fluorobenzaldehyde → 1-(4-Chloro-3-fluorophenyl)ethan-1-ol

https://huagongshe.com/reaction/1241478

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chloro-3-FluorobenzaldehydeHCID 2724985—
反応物HCID 178418348HCID 178418348—
溶媒TetrahydrofuranHCID 8028—
生成物1-(4-Chloro-3-fluorophenyl)ethan-1-olHCID 21934744—

反応手順

4-Chloro-3-fluoro-benzaldehyde (5.14 g, 32.4 mmol) was dissolved in THF (100 mL) and place at −78° C. under nitrogen atmosphere. Methyl Lithium (1.6 M in diethyl ether, 22.3 mL) was added to the reaction during a period of 3 minutes maintianing the same temperature. After the addition, the reaction was stirred at room temperature for 1 h. Then, the reaction was poured over ice water and extracted with ethyl acetate and hydrochloric acid 1N. The organic layer was collected, dried with sodium sulfate, filtered and concentrated under vacuum to produce a crude, which it was chromatograph over silica gel using 50% hexane-ethyl Acetate as solvent to yield 5.1 g of 1-(4-chloro-3-fluoro-phenyl)-ethanol. 1H NMR (400 MHz, Cl3CD) δ 7.37 (t, J=8.14 Hz, 1H), 7.20 (dd, J=1.86, 10.00 Hz, 1H), 7.09 (dd, J=1.86, 8.14 Hz, 1H), 4.89 (m, 1H), 1.93 (br s, 1H), 1.49 (d, J=6.51, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07115598B2
出典データセットuspto-grants-2006_10
ORD IDord-a41fc73086974eb095e87469a8d4e5f7
出典メモuspto-grants-2006_10