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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38242생성일: 2026년 10월 25일

Acetic Acid → 3-Chloro-4-(3-chlorophenoxy)aniline

https://huagongshe.com/reaction/38242

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물2-Chloro-1-(3-chlorophenoxy)-4-nitrobenzeneHCID 275207—
촉매IronHCID 23925—
용매Water ethanolHCID 19096565—
생성물3-Chloro-4-(3-chlorophenoxy)anilineHCID 17605534100%

반응 단계

According to Scheme 3 Step 2: A suspension of iron (5.07 mmol, 283 mg), acetic acid (1.22 mmol, 70 μL) and of 2-chloro-1-(3-chlorophenoxy)-4-nitrobenzene (1.02 mmol, 288 mg) in water/EtOH (1:1, 8 mL) was stirred at 80° C. for 30 minutes. After evaporation of EtOH, the aqueous phase was basified with a saturated solution of NaHCO3 and was extracted with AcOEt. The organic phase was washed with brine, was dried over MgSO4, was filtered and was concentrated under reduced pressure to yield 3-chloro-4-(3-chlorophenoxy)aniline (1.02 mmol, 258 mg, 100%) as a solid. The product was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524726B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-077c9c4ea8274fb796a20617fa6ba2d7
출처 메모uspto-grants-2013_09