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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 59884생성일: 2026년 10월 24일

Triphenylphosphine → tert-butyl (R)-3-(2-ethoxyphenoxy)piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/59884

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물2-EthoxyphenolHCID 66755—
반응물tert-butyl (3S)-3-hydroxypiperidine-1-carboxylateHCID 1514399—
반응물Diisopropyl azodicarboxylateHCID 5363146—
용매TolueneHCID 1140—
생성물tert-butyl (R)-3-(2-ethoxyphenoxy)piperidine-1-carboxylateHCID 13173706845.9%

반응 단계

To a solution of 2-ethoxyphenol (13.72 g, 99 mmol), tert-butyl (S)-3-hydroxypiperidine-1-carboxylate (20 g, 99 mmol), and triphenylphosphine (29 g, 111 mmol) in toluene (150 mL) at 20-25° C. was added a solution of DIAD (20 mL, 104 mmol) in toluene (50 mL) over 2 hours. After 2 hours, the reaction mixture was filtered and washed with diethyl ether (300 mL). The filtrate was washed with 3N NaOH (150 mL), dried over Na2SO4, and concentrated. The crude residue was purified via column chromatography to afford tert-butyl (R)-3-(2-ethoxyphenoxy)piperidine-1-carboxylate (14.6 g, 45%). MS (ES+) 222.2 (M-100+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440949B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-84c2c17968264ec79a61826a50901a96
출처 메모uspto-grants-2016_09