돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8701생성일: 2026년 10월 24일

Acetic Acid → 1-benzyl-N,4-dimethylpiperidin-3-amine

https://huagongshe.com/ko/reaction/8701

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물MethanolHCID 887—
반응물MethylamineHCID 6329—
반응물1-Benzyl-4-methylpiperidin-3-oneHCID 12084828—
용매TetrahydrofuranHCID 8028—
생성물1-benzyl-N,4-dimethylpiperidin-3-amineHCID 994388969%

반응 단계

To a stirred solution of 1-benzyl-4-methyl-piperidin-3-one (2.3 grams, 11.5 mmol), prepared by the methods of Iorio, M. A. and Damia, G., Tetrahedron, 26, 5519 (1970) and Grieco et al., Journal of the American Chemical Society, 107, 1768 (1985), (modified using 5% methanol as a co-solvent), both references are incorporated by reference in their entirety, dissolved in 23 mL of 2 M methylamine in tetrahydrofuran was added 1.4 mL (23 mmol) of acetic acid and the resulting mixture stirred in a sealed tube for 16 hours at room temperature. Triacetoxy sodium borohydride (4.9 grams, 23 mmol) was added and the new mixture stirred at room temperature in a sealed tube for 24 h, at which time, the reaction was quenched upon addition of 1 N sodium hydroxide (50 mL). The reaction mixture was then extracted 3×80 mL with ether, the combined ether layers dried over sodium sulfate (Na2SO4) and concentrated to dryness in vacuo affording 1.7 grams (69%) of the title compound as a white solid. LRMS: 219.1 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091208B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-8210397d84ee46a398b1d1f423bf0696
출처 메모uspto-grants-2006_08