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HRID 1855054作成日:2026年10月26日

2-(1-(3-(tetrahydro-2H-pyran-2-yloxy)phenyl)-2-oxabicyclo[2.2.2]octan-4-yl)ethanol → 3-(1-(3-Phenoxyphenyl)-2-oxabicyclo[2.2.2]octan-4-yl)propanal

https://huagongshe.com/reaction/1855054

反応式

関与物質

役割名称HCID仕込み量
反応物2-(1-(3-(tetrahydro-2H-pyran-2-yloxy)phenyl)-2-oxabicyclo[2.2.2]octan-4-yl)ethanolHCID 90408134—
反応物3-(1-(3-(tetrahydro-2H-pyran-2-yloxy)phenyl)-2-oxabicyclo[2.2.2]octan-4-yl)propanalHCID 90408392—
反応物2-(1-(3-Phenoxyphenyl)-2-oxabicyclo[2.2.2]octan-4-yl)ethanolHCID 90408877—
生成物3-(1-(3-Phenoxyphenyl)-2-oxabicyclo[2.2.2]octan-4-yl)propanalHCID 90408318—

反応手順

3-(1-(3-Phenoxyphenyl)-2-oxabicyclo[2.2.2]octan-4-yl)propanal (clear oil) was prepared using a procedure analogous to 3-(1-(3-(tetrahydro-2H-pyran-2-yloxy)phenyl)-2-oxabicyclo[2.2.2]octan-4-yl)propanal except that 2-(1-(3-(tetrahydro-2H-pyran-2-yloxy)phenyl)-2-oxabicyclo[2.2.2]octan-4-yl)ethanol was replaced with 2-(1-(3-phenoxyphenyl)-2-oxabicyclo[2.2.2]octan-4-yl)ethanol. LCMS, [M−H]+=335.2. 1H NMR (500 MHz, CDCl3) δ 9.78 (t, J=1.5 Hz, 1H), 7.34-7.23 (m, 3H), 7.14-7.03 (m, 3H), 7.01-6.95 (m, 2H), 6.87-6.81 (m, 1H), 3.81-3.78 (m, 2H), 2.43-2.36 (m, 2H), 2.09-1.94 (m, 4H), 1.69-1.58 (m, 4H), 1.54-1.47 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08962660B2
出典データセットuspto-grants-2015_02
ORD IDord-f2358af6fd7e450da216ab72954fd453
出典メモuspto-grants-2015_02