Potassium Phosphate, Tribasic → HCID 66760548、化合物

HRID 2063831ノート

反応式

HRID 2063831 の反応式
P([O-])([O-])([O-])=O.[K+].[K+].[K+].[CH3:9][C:10]1([CH3:20])[CH2:14][C:13]2[CH:15]=[CH:16][CH:17]=[C:18]([CH3:19])[C:12]=2[O:11]1.B([O-])([O-])O[C:23]1[CH:28]=[CH:27][C:26]([CH3:29])=[CH:25][CH:24]=1>Cl[Ni](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(C)C=CC=CC=1>[CH3:9][C:10]1([CH3:20])[CH2:14][C:13]2[CH:15]=[CH:16][C:17]([C:23]3[CH:28]=[CH:27][C:26]([CH3:29])=[CH:25][CH:24]=3)=[C:18]([CH3:19])[C:12]=2[O:11]1

参加物

7

反応物 3

HCID 62657Potassium Phosphate, TribasicHCID 141573Benzofuran, 2,3-dihydro-2,2,7-trimethyl-HCID 866453334-Methylphenyl borate

生成物 1

HCID 66760548HCID 66760548、化合物収率 943.9%

試薬・触媒・溶媒 3

HCID 11776Triphenylphosphine触媒HCID 178418751HCID 178418751、化合物触媒HCID 1140Toluene溶媒

実験手順

Tripotassium phosphate (28.1 g, 132 mmol) was added to a solution of toluene (200 mL) containing 2,2,7-trimethyl-2,3-dihydro-1-benzofuran (10.0 g, 5.08 mmol) synthesized in Reference Example 155, bis(triphenylphosphine)nickel (II) dichloride (0.998 g, 1.53 mmol), triphenylphosphine (0.800 g, 3.05 mmol) and 4-methylphenyl borate (8.99 g, 66.1 mmol), and the mixture was stirred under heated reflux for 2 hours. After cooled to room temperature, the reaction solution was filtered using Celite. Water was added to the obtained filtrate, and it was subjected to extraction using ethyl acetate. The extract was dried using anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. After that, the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate 20:1) to give 12.1 g of the title compound as a brown solid (yield: 94%).

後処理

  1. temperatureunder heated
  2. temperaturereflux for 2 hours
  3. filtrationthe reaction solution was filtered
  4. additionWater was added to the obtained filtrate, and it
  5. extractionwas subjected to extraction
  6. customThe extract was dried
  7. customthe solvent was removed under reduced pressure
  8. customAfter that, the obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate 20:1)

出典と根拠

ORDレコード
ord-65e17b325e5e49619f6bfc21c9a1076e
出典データセット
uspto-grants-2012_10
特許番号
US08288390B2

反応ノート

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