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HRID 2404148作成日:2026年10月27日

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

https://huagongshe.com/reaction/2404148

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物4-(Trifluoromethyl)cyclohexan-1-olHCID 2779765—
反応物Diisopropyl azodicarboxylateHCID 5363146—
反応物Methyl 1-((6-hydroxynaphthalen-2-yl)methyl)azetidine-3-carboxylateHCID 66925934—
溶媒TolueneHCID 1140—
生成物Methyl 1-((6-(4-(trifluoromethyl)cyclohexyloxy)naphthalen-2-yl)methyl)azetidine-3-carboxylateHCID 6692646528%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08802659B2
出典データセットuspto-grants-2014_08
ORD IDord-5d32f19a0448476d9835a5990fd3f501
出典メモuspto-grants-2014_08