돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 399303생성일: 2026년 10월 26일

Piperidine → 1-(Naphthalen-2-yl)piperidine

https://huagongshe.com/reaction/399303

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물2-Naphthyl TrifluoromethanesulfonateHCID 4546341—
반응물Sodium t-butoxideHCID 23676156—
반응물HCID 178506046HCID 178506046—
촉매Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
촉매(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
용매TolueneHCID 1140—
생성물1-(Naphthalen-2-yl)piperidineHCID 23070977%

반응 조건

온도105 °C

반응 단계

The method described in this example is representative of method "A". Into a screw-capped test tube were weighed 8.6 mg (0.015 mmol) Pd(dba)2, 12.8 mg (0.023 mmol) DPPF, and 44.3 mg (0.462 mmol) sodium t-butoxide (NaO-t-Bu). The solid materials were suspended in 8 ml of toluene. 2-Naphthyltriflate (85.0 mg, 0.308 mmol) was dissolved in 1 ml of toluene and added to the test tube. The test tube was sealed with a cap containing a polytetrafluoroethylene (PTFE) septum and removed from the dry box. Piperidine (40.0 μl, 0.462 mmol) was added to the test tube by syringe. The reaction mixture was heated at 105° C. for 5 hours. Thin layer chromatography (TLC) of the reaction mixture indicated complete consumption of the naphthyltriflate. The reaction mixture was cooled to room temperature, and the volatile materials were removed by rotary evaporation. Sublimation (120° C., 0.1 torr) of the resulting residue afforded N-(2-naphthyl)piperidine as a white solid (50.0 mg, 77% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05817877
출처 데이터셋uspto-grants-1998_10
ORD IDord-e8569e87b83f41cf84c4832f320de4b8
출처 메모uspto-grants-1998_10