戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 488430作成日:2026年10月26日

Hydrochloric Acid → 2-Chloro-6-ethoxybenzylamine

https://huagongshe.com/reaction/488430

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物BoraneHCID 6331—
反応物2-Chloro-6-ethoxybenzonitrileHCID 22270929—
反応物HCID 178418361HCID 178418361—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物2-Chloro-6-ethoxybenzylamineHCID 2227133764%

反応手順

To a solution of 2-chloro-6-ethoxybenzonitrile, 135, (93.2 g, 0.513 mol) in THF (350 mL) at room temperature under a dry nitrogen atmosphere was added borane in THF (1.0 M, 620 mL, 0.62 mol). The resulting mixture was heated to reflux for 3 hours and then cooled to room temperature. Water (250 mL) was added very slowly to the solution allowing for the evolution of hydrogen. Concentrated HCl (50 mL) was then added over several minutes and the solution was heated to 50° C. for 2 hours. The mixture was cooled and partitioned between chloroform and water. The aqueous layer was washed 6 times with chloroform. The combined organic fractions were washed with HCl (1 M) and this organic layer was discarded. Chloroform was added to the combined aqueous layers and solid KOH was added until the aqueous phase was basic (pH>9). The aqueous layer washed with chloroform an additional five times. The organic fractions were combined and washed with water, brine, and dried over MgSO4 and silica gel (2 g). This mixture was filtered and the filtrate was concentrated under reduced pressure to give 2-chloro-6-ethoxybenzylamine, 136, (60.1 g, 64% yield) as a light yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06972296B2
出典データセットuspto-grants-2005_12
ORD IDord-119c52be47e74176a71cbd6219f1a0d5
出典メモuspto-grants-2005_12