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3-Nitrophenol → Nitro-3-[2-(4-cyanophenyl)ethoxy]benzene

HRID 325027
ノート
印刷プレビュー

反応式

HRID 325027 の反応式
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CCOC(/N=N/C(OCC)=O)=O.[N+:32]([C:35]1[CH:36]=[C:37]([OH:41])[CH:38]=[CH:39][CH:40]=1)([O-:34])=[O:33].[C:42]([C:44]1[CH:49]=[CH:48][C:47]([CH2:50][CH2:51]O)=[CH:46][CH:45]=1)#[N:43]>C1COCC1.O>[N+:32]([C:35]1[CH:40]=[CH:39][CH:38]=[C:37]([O:41][CH2:51][CH2:50][C:47]2[CH:48]=[CH:49][C:44]([C:42]#[N:43])=[CH:45][CH:46]=2)[CH:36]=1)([O-:34])=[O:33]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 111373-NitrophenolHCID 11776TriphenylphosphineHCID 28008154-(2-Hydroxyethyl)benzonitrileHCID 5462977Diethyl azodicarboxylate

生成物 1

HCID 22033514Nitro-3-[2-(4-cyanophenyl)ethoxy]benzene収率 32%

試薬・触媒・溶媒 2

HCID 962Water
溶媒
HCID 8028Tetrahydrofuran溶媒

実験手順

Triphenylphosphine (11.3 g; 43.1 mmol) and diethylazodicarboxylate (7.5 g; 43 mmol) were dissolved in THF (250 mL) under nitrogen at 0° C. After 5 minutes, 3-nitrophenol (5.00 g; 35.9 mmol) and 2-(4-cyanophenyl)ethanol (6.3 g; 43 mmol) were added. The cooling bath was removed and the mixture stirred for 2 days at room temperature. A new batch was prepared as above and the two were combined before work-up. Water was added and the THF was evaporated. The mixture was extracted with EtOAc, and the organic phase was washed with aqueous 0.2M NaOH and brine, dried (Na2SO4) and the solvent removed in vacuo. Purification by flash chromatography (SiO2; toluene) and recrystallization from CH2Cl2:EtOH afforded 3.07 g (32%) of the sub-title compound.

後処理

  1. customThe cooling bath was removed
  2. customA new batch was prepared as above and the two
  3. customthe THF was evaporated
  4. extractionThe mixture was extracted with EtOAc
  5. washthe organic phase was washed with aqueous 0.2M NaOH and brine
  6. dry with materialdried (Na2SO4)
  7. customthe solvent removed in vacuo
  8. customPurification
  9. customby flash chromatography (SiO2; toluene) and recrystallization from CH2Cl2

出典と根拠

ORDレコード
ord-5a2211590a334c419b0a814e788018ae
出典データセット
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06221898B1

反応ノート

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