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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2404148생성일: 2026년 10월 26일

Triphenylphosphine → Methyl 1-((6-(4-(trifluoromethyl)cyclohexyloxy)naphthalen-2-yl)methyl)azetidine-3-carboxylate

https://huagongshe.com/reaction/2404148

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물4-(Trifluoromethyl)cyclohexan-1-olHCID 2779765—
반응물Diisopropyl azodicarboxylateHCID 5363146—
반응물Methyl 1-((6-hydroxynaphthalen-2-yl)methyl)azetidine-3-carboxylateHCID 66925934—
용매TolueneHCID 1140—
생성물Methyl 1-((6-(4-(trifluoromethyl)cyclohexyloxy)naphthalen-2-yl)methyl)azetidine-3-carboxylateHCID 6692646528%

반응 단계

To a vial was added methyl 1-((6-hydroxynaphthalen-2-yl)methyl)azetidine-3-carboxylate (271 mg, 1.0 mmol), 4-(trifluoromethyl)cyclohexanol (252 mg, 1.5 mmol, 1.5 equiv), PPh3 (524 mg, 2.0 mmol, 2.0 equiv) and toluene (0.8 mL) under N2 atmosphere. While stirring, DIAD (404 mg, 2.0 mmol, 2.0 equiv) was added to the reaction mixture quickly at r.t and stirred for 10 min. The reaction mixture was then purified by silica gel chromatography (PE:EA=5:1) to give the title compound (114 mg, 28%) as a slight yellow oil. ESI-MS (M+1)+: 408.2. 1H NMR (400 MHz, CD3OD) δ: 7.76 (d, 1H), 7.70 (d, 1H), 7.66 (s, 1H), 7.36 (dd, 1H), 7.24 (d, 1H), 7.17 (dd, 1H), 4.86-4.76 (m, 1H), 3.74 (s, 2H), 3.70 (s, 3H), 3.56-3.51 (m, 2H), 3.32-3.34 (m, 3H), 2.33-2.22 (m, 1H), 2.20 (d, 2H), 1.82-1.67 (m, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08802659B2
출처 데이터셋uspto-grants-2014_08
ORD IDord-5d32f19a0448476d9835a5990fd3f501
출처 메모uspto-grants-2014_08