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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1058778생성일: 2026년 10월 27일

Acetaldehyde → Phenyl-piperidin-4-yl-methanol

https://huagongshe.com/reaction/1058778

반응식

참여 물질

역할이름HCID투입량
반응물AcetaldehydeHCID 177—
반응물Sodium ChlorideHCID 5234—
반응물Sodium HydroxideHCID 14798—
반응물Phenyl(piperidin-4-yl)methanoneHCID 226102—
용매DichloromethaneHCID 6344—
생성물Phenyl-piperidin-4-yl-methanolHCID 33908690%

반응 조건

온도3.5 °C

반응 단계

4-benzoyl-piperidine (2.0 g, 10.6 mmol) was added over a solution of 6.8 g of (+)-B-chlorodiisopinocanfeilboran ((+)-DIP-Cl) (21.25 mmol) in dichloromethane (20 mL, dry) cooled down to 3-4° C. After reacting for 72 h, 2.0 mL of acetaldehyde (35.46 mmol) were added and stirred at room temperature for 3 h. 24 mL of an aqueous NaOH (6N) solution, dichloromethane and saturated aqueous NaCl solution were added. The phases were separated and the usual treatment of the organic phase provided (+)-α-phenyl4-piperidinemethanol as a white solid with a m.p.=64-66° C. in a 90% yield (84% ee).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06518284B2
출처 데이터셋uspto-grants-2003_02
ORD IDord-5b340ce48bb34c8c824d98daaba40a8a
출처 메모uspto-grants-2003_02