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HRID 1515104作成日:2026年10月26日

Triphenylphosphine → 4-(3,4-Dichlorobenzyloxy)-3-fluorobenzaldehyde

https://huagongshe.com/reaction/1515104

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物3,4-Dichlorobenzyl alcoholHCID 15728—
反応物3-Fluoro-4-hydroxybenzaldehydeHCID 587250—
反応物Diethylazodicarboxylate tolueneHCID 66777355—
溶媒TetrahydrofuranHCID 8028—
生成物4-(3,4-Dichlorobenzyloxy)-3-fluorobenzaldehydeHCID 8665175080%

反応手順

3-Fluoro-4-hydroxybenzaldehyde (400 mg, 2.85 mmol), 3,4-dichlorobenzyl alcohol (665 mg, 3.76 mmol), and triphenylphosphine (980 mg, 3.74 mmol) were dissolved in tetrahydrofuran (8 mL), and a diethyl azodicarboxylate toluene solution (2.2 M, 1.71 mL, 3.76 mmol) was slowly added dropwise thereto at room temperature, and then, the resulting mixture was stirred under a nitrogen atmosphere at room temperature for 2 hours. The solvent in the reaction solution was distilled off under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=100:0 to 95:5 (v/v)), whereby the objective title compound was obtained as a colorless oily substance (680 mg, yield: 80%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08222281B2
出典データセットuspto-grants-2012_07
ORD IDord-4dd62a4d8538447393c32f3cbffb897c
出典メモuspto-grants-2012_07