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Trimethyl Phosphate → HCID 10975655、化合物

HRID 1657196
ノート
印刷プレビュー

反応式

HRID 1657196 の反応式
[OH:1][C:2]1[CH:10]=[C:9]2[C:5]([CH2:6][CH2:7][NH:8]2)=[CH:4][CH:3]=1.P(OC)(OC)(O[CH3:14])=O>C(Cl)Cl>[CH3:14][N:8]1[C:9]2[C:5](=[CH:4][CH:3]=[C:2]([OH:1])[CH:10]=2)[CH2:6][CH2:7]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 10541Trimethyl PhosphateHCID 524507Indolin-6-ol

生成物 1

HCID 10975655HCID 10975655、化合物収率 107.5%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To 37.78 g (0.286 mol) of 6-hydroxyindoline 5 in a 100 ml round-bottom flask fitted with a magnetic stirrer, thermometer and condenser connected to a source of nitrogen was added 13.38 ml (16.02 g, 0.114 mol) of trimethyl phosphate. It was then placed in an oil bath and heating was commenced. The bath temperature reached 105° in 10 min. Then the reaction mixture became homogeneous and shortly thereafter an exotherm occurred. The flask was removed periodically from the oil bath to keep the internal temperature below 150°. The reaction was heated at 140°-150° for 2 hr. Thin layer chromatography on silica gel plates eluted with 50% Ethyl acetate/hexane or 4% methanol/methylene chloride showed that starting material was still present and 3 ml (3.59 g, 25.6 mmol) more of trimethyl phosphate was added. Heating was continued at 155° for 1.5 hr. The reaction mixture was allowed to cool and then dissolved in 100 ml of saturated sodium carbonate solution and 100 ml of methylene chloride with warming in portions. The aqueous phase was separated and washed with 2×100 ml of methylene chloride. The organic phases were combined, washed with 200 ml of half-saturated brine, dried over sodium sulfate and concentrated in vacuo to leave 28.6 g (67%) of dark tar. This was dissolved in methylene chloride and filtered through 300 ml of silica gel in methylene chloride. A total of 800 ml of methylene chloride eluate and then 400 ml of ethyl acetate was collected. Concentration and collection of the residue from hexane gave 18.29 g (43%) of crude product 7 as a brown solid which was used for the preparation of 9.

後処理

  1. customthermometer and condenser connected to a source of nitrogen
  2. customIt was then placed in an oil bath
  3. temperatureheating
  4. customThe flask was removed periodically from the oil bath
  5. customthe internal temperature below 150°
  6. temperatureThe reaction was heated at 140°-150° for 2 hr
  7. washThin layer chromatography on silica gel plates eluted with 50% Ethyl acetate/hexane or 4% methanol/methylene chloride
  8. addition3 ml (3.59 g, 25.6 mmol) more of trimethyl phosphate was added
  9. temperatureHeating
  10. waitwas continued at 155° for 1.5 hr
  11. temperatureto cool
  12. dissolutiondissolved in 100 ml of saturated sodium carbonate solution
  13. temperature100 ml of methylene chloride with warming in portions
  14. customThe aqueous phase was separated
  15. washwashed with 2×100 ml of methylene chloride
  16. washwashed with 200 ml of half-saturated brine
  17. dry with materialdried over sodium sulfate
  18. concentrationconcentrated in vacuo
  19. customto leave 28.6 g (67%) of dark tar
  20. filtrationfiltered through 300 ml of silica gel in methylene chloride
  21. customA total of 800 ml of methylene chloride eluate and then 400 ml of ethyl acetate was collected
  22. concentrationConcentration and collection of the residue from hexane

出典と根拠

ORDレコード
ord-f0f090d3999a4140baf01b8f58b9f89d
出典データセット
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05256799

反応ノート

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