돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49933생성일: 2026년 10월 24일

Sodium hydride → 3-(Aminomethyl)benzoic acid hydrochloride

https://huagongshe.com/ko/reaction/49933

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물3-(Chloromethyl)benzoic acidHCID 241752—
반응물Di-tert-butyl IminodicarboxylateHCID 279800—
용매DimethylformamideHCID 6228—
생성물3-(Aminomethyl)benzoic acid hydrochlorideHCID 16218772—

반응 조건

온도80 °C

반응 단계

4.34 g (20.0 mmol) of di(t-butyl) iminodicarboxylate was added to a mixture of 800 mg (20.0 mmol) of sodium hydride (60% dispersion in mineral oil) and 50 ml of dimethylformamide. 1.71 g (10.0 mmol) of 3-chloromethylbenzoic acid was added to the obtained mixture, and they were stirred at 80° C. for 2 hours. After the concentration under reduced pressure, 40 ml of dioxane containing 4 M of hydrogen chloride was added to the residue, and they were stirred at room temperature overnight. A white precipitate thus formed was taken by the filtration and washed with ethyl acetate to obtain 3-aminomethylbenzoic acid hydrochloride as white crystals. A mixture of this aminomethyl compound, 10 ml of water, 10 ml of 28% aqueous ammonia and 3.00 g (71.4 mmol) of cyanamide was stirred at 60° C. for 7 days. The solvent was evaporated, and the residue was purified by the reversed-phase HPLC in the same manner as that in step 5 in Example 1 to obtain the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710056B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-db7ee05540cf44fa9363b18f21aa4401
출처 메모uspto-grants-2004_03