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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 331072생성일: 2026년 10월 25일

Acetic Acid → (2S,5R)-1-benzyl-2,5-dimethyl-4-(3,3,3-trifluoropropyl)piperazine

https://huagongshe.com/reaction/331072

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물3,3,3-TrifluoropropanalHCID 68028—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물(2S,5R)-1-Benzyl-2,5-dimethylpiperazineHCID 23402345—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물(2S,5R)-1-benzyl-2,5-dimethyl-4-(3,3,3-trifluoropropyl)piperazineHCID 5751919792.4%

반응 단계

To a solution of (2S,5R)-1-benzyl-2,5-dimethylpiperazine (2.00 g, 7.21 mmol) in THF (10 mL), MeOH (10 mL), and TEA (1.0 mL) was added 3,3,3-trifluoropropionaldehyde (1.62 g, 14.4 mmol) and AcOH (0.826 mL, 14.4 mmol) followed by sodium cyanoborohydride (0.907 g, 14.4 mmol). The reaction was allowed to stir for 2 h, at which time the reaction was quenched with water (15 mL) then made basic with NaHCO3 and extracted with EtOAc. The organic layer was washed with brine, dried and concentrated in vacuo to yield a white powder (2.0 g, 90%). Mass Spectrum: Calcd for C16H24N2F3 (M+H): 301. Found: 301.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08877761B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-5fb63c3cc11c4bfaa5073acd941316eb
출처 메모uspto-grants-2014_11