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Water → HCID 86615888, 화합물

HRID 602213
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인쇄 미리보기

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HRID 602213 반응식
C(=O)([O-])[O-].[K+].[K+].[Cl:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]2[CH:19]=[CH:18][C:17]([CH2:20][O:21][CH:22]3[CH2:27][CH2:26][CH2:25][NH:24][CH2:23]3)=[CH:16][CH:15]=2)=[CH:10][CH:9]=1.F[C:29]1[CH:36]=[CH:35][CH:34]=[CH:33][C:30]=1[CH:31]=[O:32].O>[I-].C([N+](CCCC)(CCCC)CCCC)CCC.CN(C)C=O>[Cl:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]2[CH:19]=[CH:18][C:17]([CH2:20][O:21][CH:22]3[CH2:27][CH2:26][CH2:25][N:24]([C:36]4[CH:29]=[C:30]([CH:33]=[CH:34][CH:35]=4)[CH:31]=[O:32])[CH2:23]3)=[CH:16][CH:15]=2)=[CH:10][CH:9]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 67970o-FluorobenzaldehydeHCID 589926553-[(4'-Chlorobiphenyl-4-yl)methoxy]piperidine

생성물 1

HCID 86615888HCID 86615888, 화합물수율 53%

시약·촉매·용매 2

HCID 67553Tetrabutylammonium Iodide
촉매
HCID 6228Dimethylformamide용매

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온도
100 °C

실험 절차

Tetrabutylammonium iodide (26.9 mg, 0.0729 mmol) and potassium carbonate (206 mg, 1.46 mmol) were added to a solution of 3-[(4′-chlorobiphenyl-4-yl)methoxy]piperidine (220 mg, 0.729 mmol) and 2-fluorobenzaldehyde (0.159 mL, 1.46 mmol) in N,N-dimethylformamide (5 mL). The mixture was stirred at 100° C. for 8 hours. Subsequently, water was added and the mixture was extracted with ethyl acetate and washed with brine. The washed product was dried over magnesium sulfate and the solvent was evaporated. Purification of the resulting residue by silica gel column chromatography (hexane:ethyl acetate=40:1->10:1) gave 156 mg (53%) of the desired compound as a pale yellow powder.

후처리

  1. extractionthe mixture was extracted with ethyl acetate
  2. washwashed with brine
  3. dry with materialThe washed product was dried over magnesium sulfate
  4. customthe solvent was evaporated
  5. customPurification of the resulting residue by silica gel column chromatography (hexane:ethyl acetate=40:1->10:1)

출처 및 근거

ORD 기록
ord-aa0b40b1bb7545c387930c3dda8f5de9
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07902367B2

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