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

HRID 399303

반응식

HRID 399303 반응식
CC(C)([O-])C.[Na+].[CH:7]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=[CH:9][C:8]=1OS(C(F)(F)F)(=O)=O.[NH:25]1[CH2:30][CH2:29][CH2:28][CH2:27][CH2:26]1>C1(C)C=CC=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.[Fe+2]>[CH:7]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=[CH:9][C:8]=1[N:25]1[CH2:30][CH2:29][CH2:28][CH2:27][CH2:26]1

참가 물질

8

반응 조건

온도
105 °C

실험 절차

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).

후처리

  1. customInto a screw-capped test tube were weighed
  2. additionadded to the test tube
  3. customThe test tube was sealed with a cap
  4. customremoved from the dry box
  5. customconsumption of the naphthyltriflate
  6. temperatureThe reaction mixture was cooled to room temperature
  7. customthe volatile materials were removed by rotary evaporation

출처 및 근거

ORD 기록
ord-e8569e87b83f41cf84c4832f320de4b8
출처 데이터셋
uspto-grants-1998_10
특허 번호
US05817877

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