Water → Methyl alpha-Methyl-9-nitro-9,10-dihydroanthracene-10-acetate

HRID 373738

反応式

HRID 373738 の反応式
[N+:1]([C:4]1[C:5]2[C:10]([CH:11]=[C:12]3[C:17]=1[CH:16]=[CH:15][CH:14]=[CH:13]3)=[CH:9][CH:8]=[CH:7][CH:6]=2)([O-:3])=[O:2].CN([S+](N(C)C)N(C)C)C.C[Si-](F)(F)(C)C.OP([O-])(O)=O.[K+].[OH2:40].[CH2:41]1[CH2:45][O:44][CH2:43][CH2:42]1>C(#N)C.CCOCC>[CH3:41][CH:42]([CH:11]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]([N+:1]([O-:3])=[O:2])[C:17]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]1=2)[C:43]([O:44][CH3:45])=[O:40]

参加物

8

実験手順

To a solution of 0.757 g (3.39 mmol) of 9-nitroanthracene and 0.663 mL (3.56 mmol) of MTS in 20 mL of anhydrous THF was added 0.941 g (3.42 mmol) of TASF in 2 mL of anhydrous acetonitrile at -78° C. The mixture was stirred for 24 hr. at -78° C. Then, ten mL of saturated KH2PO4 and 20 mL of water were added, the mixture was warmed to room temperature, and the product was extracted into ether. The combined ether extract was washed with water, dried, and concentrated. The major product, 0.491 g (56%), was isolated by column chromatography on silica using 20° ether/hexane as the solvent. Addition of small amount of ether to the major fraction yielded a light yellow solid. The product was analyzed by ultraviolet absorption, infrared spectroscopy, nuclear magnetic resonance spectroscopy, and mass spectrometry.

後処理

  1. customat -78° C
  2. extractionthe product was extracted into ether
  3. extractionThe combined ether extract
  4. washwas washed with water
  5. customdried
  6. concentrationconcentrated
  7. customThe major product, 0.491 g (56%), was isolated by column chromatography on silica using 20° ether/hexane as the solvent
  8. customyielded a light yellow solid
  9. customThe product was analyzed by ultraviolet absorption

出典と根拠

ORDレコード
ord-d9fb702a329145de8abc98b5cb936f4b
出典データセット
uspto-grants-1992_11
特許番号
US05164499

関連ノート

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