돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 489745생성일: 2026년 10월 24일

Methylamine → (2R)-(4E)-N-Methyl-5-(3-pyridyl)-4-penten-2-amine

https://huagongshe.com/ko/reaction/489745

반응식

참여 물질

역할이름HCID투입량
반응물MethylamineHCID 6329—
반응물(2S)-(4E)-5-(3-pyridyl)-4-penten-2-ol p-toluenesulfonateHCID 87465994—
생성물(2R)-(4E)-N-Methyl-5-(3-pyridyl)-4-penten-2-amineHCID 9898976—

반응 조건

온도105 °C

반응 단계

A mixture of (2S)-(4E)-5-(3-pyridyl)-4-penten-2-ol p-toluenesulfonate (3.80 g, 11.97 mmol) and methylamine (20 mL, 2.0M solution in THF) was heated at 100-110° C. for 8 h in a sealed glass tube. The mixture was cooled to ambient temperature and concentrated under reduced pressure on a rotary evaporator. The resulting brown syrup was diluted with saturated NaHCO3 solution (25 mL) and extracted with chloroform (4×25 mL). The combined chloroform extracts were dried (K2CO3), filtered, and concentrated by rotary evaporation to afford a thick, brown syrup (2.00 g). The crude product was purified by column chromatography on silica gel, eluting with chloroform-methanol (95:5, v/v). Selected fractions were combined, concentrated by rotary evaporation affording a 800 mg (37.9%) of a pale-yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06979695B2
출처 데이터셋uspto-grants-2005_12
ORD IDord-c1f47da3d71b446ca9c2f525bf45ecc5
출처 메모uspto-grants-2005_12