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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128912생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/128912

반응식

참여 물질

역할이름HCID투입량
반응물1-Phenyl-1-propanolHCID 7147—
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물2-hydroxy-alpha-(1-imidazolyl)benzaldehyde O-methyloximeHCID 135976165—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물alpha-(1-imidazolyl)-2-(1-phenylpropyloxy)benzaldehyde O-methyloximeHCID 5451549394.9%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05466661
출처 데이터셋uspto-grants-1995_11
ORD IDord-4d2ce26ab71a473abd85b8cc9ab46a21
출처 메모uspto-grants-1995_11