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Sodium hydride → HCID 19381508, 화합물

HRID 2209738
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HRID 2209738 반응식
[OH:1][C:2]1[CH:16]=[CH:15][C:5]([C:6]([N:8]([CH:12]([CH3:14])[CH3:13])[CH:9]([CH3:11])[CH3:10])=[O:7])=[CH:4][C:3]=1[O:17][CH3:18].[H-].[Na+].[C:21]([C:23]1[CH:34]=[CH:33][C:26]([O:27][CH2:28][CH2:29][CH2:30][CH2:31]Cl)=[CH:25][CH:24]=1)#[N:22]>CN(C)C=O>[C:21]([C:23]1[CH:34]=[CH:33][C:26]([O:27][CH2:28][CH2:29][CH2:30][CH2:31][O:1][C:2]2[CH:16]=[CH:15][C:5]([C:6]([N:8]([CH:9]([CH3:11])[CH3:10])[CH:12]([CH3:13])[CH3:14])=[O:7])=[CH:4][C:3]=2[O:17][CH3:18])=[CH:25][CH:24]=1)#[N:22]
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HCID 24758Sodium hydrideHCID 19381506HCID 19381506, 화합물HCID 217472594-Hydroxy-3-methoxy-N,N-di(propan-2-yl)benzamide

생성물 1

HCID 19381508HCID 19381508, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
0 °C

실험 절차

A stirred solution of 4-hydroxy-3-methoxy-N,N-bis(1-methylethyl)benzamide (1.0 g, 4.0 mmol) in 50 mL of N,N-dimethylformamide is treated with 60% sodium hydride (160 mg, 4.0 mmol). After stirring at 0° C. for 10 minutes, the reaction is treated with 4-(4-cyanophenoxy)butyl chloride (835 mg, 4.0 mmol) and stirred at 60° C. for 4 days. The reaction is partitioned between diethyl ether and water. The organic layer is washed with brine, dried over magnesium sulfate, and concentrated in vacuo. The resulting material is purified by chromatography on silica gel (30 g) with 60 % ethyl acetate/hexane as the eluent to afford 4-[4-(4-cyanophenoxy)butoxy]-3-methoxy-N,N-bis(1-methylethyl)benzamide as an oil.

후처리

  1. stirringstirred at 60° C. for 4 days
  2. customThe reaction is partitioned between diethyl ether and water
  3. washThe organic layer is washed with brine
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated in vacuo
  6. customThe resulting material is purified by chromatography on silica gel (30 g) with 60 % ethyl acetate/hexane as the eluent

출처 및 근거

ORD 기록
ord-0301d4a6d49f46cdab83449a008b4330
출처 데이터셋
uspto-grants-1995_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05455274

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