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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44216생성일: 2026년 10월 24일

Ammonia → 2-(4-Nitrophenyl)ethanimidamide hydrochloride

https://huagongshe.com/ko/reaction/44216

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Hydrochloric AcidHCID 313—
반응물EthanolHCID 702—
반응물1,4-DioxaneHCID 31275—
반응물p-NitrophenylacetonitrileHCID 68386—
용매MethanolHCID 887—
생성물2-(4-Nitrophenyl)ethanimidamide hydrochlorideHCID 46318421—

반응 단계

A suspension of (4-nitrophenyl)acetonitrile (4.86 g, 30.0 mmol) in ethanol (6 mL, 99 mmol) in a 250 mL round bottom flask was slowly treated at room temperature with 4N hydrochloric acid in dioxane (38 mL, 152 mmol) and stirred for 22 hours. After carefully removing the solvent under water aspirator vacuum at 40° C. the obtained wet pale yellow product was suspended in 21 mL ethanol. Then, a 7N ammonia solution in methanol (12 mL, 84 mmol) was slowly added giving a pale gray suspension. After stirring for two hours additional 2 mL (14 mmol) 7N ammonia solution in methanol were added. After further stirring for one hour at room temperature all volatiles were removed under water aspirator vacuum at 40° C. To remove residues of ethanol and dioxane methyl t-butyl ether (30 mL) was added and once more all volatiles were removed under water aspirator vacuum at 40° C. giving an off-white solid. The crude product was used without purification in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541419B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-e6029c687e9b4c9f90cc2974bd4cd2cd
출처 메모uspto-grants-2013_09