Acetic Acid → 9H-Xanthene-9-methanamine

HRID 1057415

反応式

HRID 1057415 の反応式
[Na].[CH:2]1[C:15]2[CH:14]([C:16]([NH2:18])=O)[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[O:7][C:6]=2[CH:5]=[CH:4][CH:3]=1.C(O)(=O)C>O1CCOCC1>[NH2:18][CH2:16][CH:14]1[C:15]2[CH:2]=[CH:3][CH:4]=[CH:5][C:6]=2[O:7][C:8]2[C:13]1=[CH:12][CH:11]=[CH:10][CH:9]=2

参加物

5

実験手順

To a stirred suspension of sodium boronhydride (1.89 g, 50 mmol) and 9-xanthencarboxamide (2.25 g, 10 mmol) in dioxane (20 mL) was added acetic acid (3.0 g, 50 mmol) in dioxane (10 mL) over a period of 10 minutes at 10° C.; the reaction mixture was stirred at reflux for 2 hours. The reaction mixture was concentrated to dryness in vacuo, excess reagent was decomposed with water and the solution extracted with chloroform. The extract was washed with water and dried over anhydrous sodium sulphate. The chloroform layer was evaporated in vacuo and the residue was purified by silica gel column chromatography (ethylacetate:methanol, 9:1 as eluent) to give a white solid (1.6 g, 7.6 mmol) in 76.2% yield.

後処理

  1. temperatureat reflux for 2 hours
  2. concentrationThe reaction mixture was concentrated to dryness in vacuo, excess reagent
  3. extractionthe solution extracted with chloroform
  4. washThe extract was washed with water
  5. dry with materialdried over anhydrous sodium sulphate
  6. customThe chloroform layer was evaporated in vacuo
  7. customthe residue was purified by silica gel column chromatography (ethylacetate:methanol, 9:1 as eluent)

出典と根拠

ORDレコード
ord-8631a093844c4bcda97fa096314d8327
出典データセット
uspto-grants-2003_02
特許番号
US06514983B1

関連ノート

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