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HRID 128912作成日:2026年10月27日

1-Phenyl-1-propanol → alpha-(1-imidazolyl)-2-(1-phenylpropyloxy)benzaldehyde O-methyloxime

https://huagongshe.com/reaction/128912

反応式

関与物質

役割名称HCID仕込み量
反応物1-Phenyl-1-propanolHCID 7147—
反応物TriphenylphosphineHCID 11776—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物2-hydroxy-alpha-(1-imidazolyl)benzaldehyde O-methyloximeHCID 135976165—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物alpha-(1-imidazolyl)-2-(1-phenylpropyloxy)benzaldehyde O-methyloximeHCID 5451549394.9%

反応手順

Triphenylphosphine (1.05 g), 1-phenylpropyl alcohol (0.54 g) and THF (20 ml) were added to 2-hydroxy-α-(1-imidazolyl)benzaldehyde O-methyloxime (0.43 g), and diethyl azodicarboxylate (0.70 g) was added under ice-cooling over 10 minutes. Then the mixture was stirred at room temperature for 2 hours. After completion of the reaction, ether (100 ml) was added, the mixture was washed with water (80 ml) twice, and the ether layer was concentrated under reduced pressure. The resulting crude product was purified by silica gel chromatography to give α-(1-imidazolyl)-2-(1-phenylpropyloxy)benzaldehyde O-methyloxime (0.63 g) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05466661
出典データセットuspto-grants-1995_11
ORD IDord-4d2ce26ab71a473abd85b8cc9ab46a21
出典メモuspto-grants-1995_11