돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 511116생성일: 2026년 10월 24일

2-Methyl-1-butene → (S)-2-methyl-3-[4-(4-trifluoromethyl-phenyl)-piperazin-1-yl]-propionic acid

https://huagongshe.com/ko/reaction/511116

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-1-buteneHCID 11240—
반응물Sodium ChloriteHCID 23668197—
반응물Monosodium phosphateHCID 23672064—
반응물(S)-2-methyl-3-[4-(4-trifluoromethyl-phenyl)-piperazin-1-yl]-propionaldehydeHCID 58576376—
용매WaterHCID 962—
용매tert-ButanolHCID 6386—
생성물(S)-2-methyl-3-[4-(4-trifluoromethyl-phenyl)-piperazin-1-yl]-propionic acidHCID 58576422—

반응 단계

(S)-2-Methyl-3-[4-(4-trifluoromethyl-phenyl)-piperazin-1-yl]-propionaldehyde (1.99 g; 6.6 mmol, prepared in accordance with Example 66) is suspended in a mixture of tert-butanol (48 mL) and water (12 mL); sodium dihydrogenphosphate (1.59 g; 13.3 mmol) and 2-methyl-butene (13.94 g; 199 mmol) are added and the resulting mixture is stirred until a solution is obtained. Sodium chlorite (1.12 g; 9.9 mmol) is added and the reaction is stirred at room temperature for one hour. The precipitate formed is filtered, is washed with water and is dried at 40° C. under 3 mbar. Aqueous sat ammonium chloride (50 mL) is added to the filtrate which is then extracted with dichloromethane (2×50 mL). The combined organic layers are washed with brine (50 mL) and concentrated under reduced pressure. The residue obtained is dried at 40° C. under 3 mbar. The enantiopure product is obtained as colourless solid (1.3 g; 4.1 mmol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09096524B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-13fb1e16d1894bcbb2bacbb075e312af
출처 메모uspto-grants-2015_08