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Cesium carbonate → (4'-Chloro-3,5-diethylbiphen-4-yl)carbamic acid tert-butyl ester

HRID 72282
ノート
印刷プレビュー

反応式

HRID 72282 の反応式
C(=O)([O-])[O-].[Cs+].[Cs+].[C:7]([O:11][C:12](=[O:25])[NH:13][C:14]1[C:19]([CH2:20][CH3:21])=[CH:18][C:17](Br)=[CH:16][C:15]=1[CH2:23][CH3:24])([CH3:10])([CH3:9])[CH3:8].[Cl:26][C:27]1[CH:32]=[CH:31][C:30](B(O)O)=[CH:29][CH:28]=1.C1(P(C2CCCCC2)C2C=CC=CC=2C2C(C(C)C)=CC(C(C)C)=CC=2C(C)C)CCCCC1>O.CC(C)=O.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[C:7]([O:11][C:12](=[O:25])[NH:13][C:14]1[C:19]([CH2:20][CH3:21])=[CH:18][C:17]([C:30]2[CH:31]=[CH:32][C:27]([Cl:26])=[CH:28][CH:29]=2)=[CH:16][C:15]=1[CH2:23][CH3:24])([CH3:10])([CH3:9])[CH3:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 10796Cesium carbonateHCID 742994-Chlorophenylboronic acidHCID 111557942-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 59450511tert-Butyl (4-bromo-2,6-diethylphenyl)carbamate

生成物 1

HCID 59450514(4'-Chloro-3,5-diethylbiphen-4-yl)carbamic acid tert-butyl ester収率 67.2%

試薬・触媒・溶媒 3

HCID 167845palladium(II) acetate触媒
HCID 180Acetone溶媒
HCID 962Water溶媒

実験手順

A solution of cesium carbonate (89.12 g, 0.27 mol) in water (600 ml) is added to a degassed solution of (4-bromo-2,6-diethylphenyl)carbamic acid tert-butyl ester (30 g, 0.091 mol) and 4-chlorophenylboronic acid (21.54 g, 0.138 mol) in acetone (3 L), and the mixture is stirred at room temperature under an atmosphere of nitrogen. Palladium acetate (1.02 g, 0.004 mol) and 2-(dicyclohexylphosphino)-2′,4′,6′-tri-iso-propyl-1,1′-biphenyl (4.33 g, 0.009 mol) are added and the reaction mixture is stirred at room temperature for 12 hours. The mixture is filtered through diatomaceous earth, and the filtrate is evaporated under reduced pressure to remove most of the acetone. The remaining solution is extracted with ethyl acetate (3×300 ml). The organic extracts are combined and concentrated under reduced pressure to give (4′-chloro-3,5-diethylbiphen-4-yl)carbamic acid tert-butyl ester (22 g).

後処理

  1. stirringthe reaction mixture is stirred at room temperature for 12 hours
  2. filtrationThe mixture is filtered through diatomaceous earth
  3. customthe filtrate is evaporated under reduced pressure
  4. customto remove most of the acetone
  5. extractionThe remaining solution is extracted with ethyl acetate (3×300 ml)
  6. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-801fd93d49f948198bd40fba334e2bc0
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08828908B2

反応ノート

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