돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30553생성일: 2026년 10월 25일

Water → 1-{[4-(Difluoromethoxy)phenyl]ethynyl}-3-propylbenzene

https://huagongshe.com/reaction/30553

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriethylboraneHCID 7357—
반응물Sodium HydroxideHCID 14798—
반응물N-[(E)-[3-[2-[4-(difluoromethoxy)phenyl]ethynyl]phenyl]methylideneamino]-4-methylbenzenesulfonamideHCID 59790336—
용매TetrahydrofuranHCID 8028—
생성물1-{[4-(Difluoromethoxy)phenyl]ethynyl}-3-propylbenzeneHCID 5743585689%

반응 단계

A mixture of N′-[(1E)-(3-{[4-(difluoromethoxy)phenyl]ethynyl}phenyl)methylene]-4-methylbenzenesulfonohydrazide (0.67 mg, 1.52 mmol) in THF was treated with triethyl borane (1.0 M in THF, 1.52 mL, 1.52 mmol), stirred for 2 minutes, treated with NaOH (2.5 N, 0.61 mL, 1.52 mmol), refluxed for 2 hours, cooled to room temperature, poured into water and extracted with EtOAc. The organic extracts were combined, dried over MgSO4 and concentrated in vacuo. The resultant residue was purified on silica gel (ISCO) using hexanes/EtOAc (50/1) as the eluting solvents to give 1-{[4-(difluoromethoxy)phenyl]ethynyl}-3-propylbenzene as a clear oil (386 mg, 89% yield), MS m/e (M+H)+ 286; 1H NMR (400 MHz, DMSO-d6) 0.85 (t, J=7.32 Hz, 3H), 1.57 (m, 2H), 2.6 (t, J=7.32 Hz, 2H), 7.2 (m, 3H), 7.35-7.45 (m, 4H), 7.58 (d, J=8.79 Hz, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423158B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-2afa4f797d6842c69a7d8f1808c9d185
출처 메모uspto-grants-2008_09