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p-Toluenesulfonic acid → HCID 68643976, 화합물

HRID 2388701
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인쇄 미리보기

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HRID 2388701 반응식
[C:1]([N:4]1[CH2:9][CH2:8][C:7](=O)[CH2:6][CH:5]1[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)(=[O:3])[CH3:2].[NH:17]1[CH2:21][CH2:20][CH2:19][CH2:18]1.CC1C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[C:11]1([CH:5]2[CH:6]=[C:7]([N:17]3[CH2:21][CH2:20][CH2:19][CH2:18]3)[CH2:8][CH2:9][N:4]2[C:1](=[O:3])[CH3:2])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6101p-Toluenesulfonic acidHCID 31268PyrrolidineHCID 575503031-Acetyl-2-phenylpiperidin-4-one

생성물 1

HCID 68643976HCID 68643976, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a mixture of 1-acetyl-2-phenylpiperidin-4-one (3.364 mmol, 1.0 eq.) and pyrrolidine (3.7 mmol, 1.1 eq.) in toluene (16 ml) was added PTSA (0.336 mmol, 0.1 eq.) and the reaction mixture was heated to reflux for 5 h using a Dean-Stark apparatus. After completion of the reaction, the solvent was evaporated under reduced pressure to obtain the crude product which was used in the next step without further purification.

후처리

  1. temperaturethe reaction mixture was heated
  2. temperatureto reflux for 5 h
  3. customAfter completion of the reaction
  4. customthe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-abe1104a17c7417c91c766dfe9bf8f03
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08268814B2

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