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HRID 546795作成日:2026年10月27日

1-Bromo-3-chloropropane → 5-Chloro-2-(2-trifluoromethylphenyl)pentanenitrile

https://huagongshe.com/reaction/546795

反応式

関与物質

役割名称HCID仕込み量
反応物1-Bromo-3-chloropropaneHCID 8006—
反応物2-(Trifluoromethyl)phenylacetonitrileHCID 76435—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物5-Chloro-2-(2-trifluoromethylphenyl)pentanenitrileHCID 66839598132%

反応条件

温度-10 °C

反応手順

(2-Trifluoromethylphenyl)acetonitrile (12.47 g, 67.3 mmol) was dissolved in THF (87.3 mL) at room temperature under nitrogen atmosphere. The reaction solution was cooled to −10° C. Then, potassium tert-butoxide (7.93 g, 70.7 mmol) was added to the reaction solution and the reaction mixture was stirred at −10° C. for 10 minutes. 1-Bromo-3-chloropropane (6.99 mL, 70.7 mmol) was added dropwise to the reaction mixture over 14 minutes, and the reaction mixture was stirred at 0° C. for 2 hours. The reaction was quenched with 10% NH4Cl aq. (8.6 mL). After the mixture was stirred, the aqueous layer was separated. The organic layer was concentrated under the reduced pressure to obtain the title compound (23.24 g). The yield was calculated as over 99% by HPLC external standard method.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07935815B2
出典データセットuspto-grants-2011_05
ORD IDord-d045f116488943008215e35a9e10d823
出典メモuspto-grants-2011_05