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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 488430생성일: 2026년 10월 25일

Hydrochloric Acid → 2-Chloro-6-ethoxybenzylamine

https://huagongshe.com/reaction/488430

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물BoraneHCID 6331—
반응물2-Chloro-6-ethoxybenzonitrileHCID 22270929—
반응물HCID 178418361HCID 178418361—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2-Chloro-6-ethoxybenzylamineHCID 2227133764%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06972296B2
출처 데이터셋uspto-grants-2005_12
ORD IDord-119c52be47e74176a71cbd6219f1a0d5
출처 메모uspto-grants-2005_12