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Ammonium Chloride → (3RS,4RS)-4-allyl-7-methoxy-3-(4-methoxyphenyl)-3-methylthiochroman

HRID 1268080
ノート
印刷プレビュー

反応式

HRID 1268080 の反応式
[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([C:7](=O)[C:8]([C:14]3[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=3)([CH3:13])[CH2:9][S:10]2)=[CH:5][CH:4]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].[Cl-].[NH4+].[CH2:31]([Si](C)(C)C)[CH:32]=[CH2:33]>O1CCCC1.O.[I-].[Zn+2].[I-].C(OCC)(=O)C.CCCCCC>[CH2:33]([CH:7]1[C:6]2[C:11](=[CH:12][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2)[S:10][CH2:9][C:8]1([C:14]1[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=1)[CH3:13])[CH:32]=[CH2:31]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

9

反応物 4

HCID 25517Ammonium ChlorideHCID 69808AllyltrimethylsilaneHCID 109799547-Methoxy-3-(4-methoxyphenyl)-3-methylthiochroman-4-oneHCID 21226445Aluminium lithium hydride

生成物 1

HCID 22033345(3RS,4RS)-4-allyl-7-methoxy-3-(4-methoxyphenyl)-3-methylthiochroman収率 60.3%

試薬・触媒・溶媒 4

HCID 9883512
zinc(II)iodide
触媒
HCID 962Water溶媒
HCID 8028Tetrahydrofuran溶媒
HCID 21226206Ethyl acetate hexane溶媒

反応条件

温度
-78 °C

実験手順

7-Methoxy-3-(4-methoxyphenyl)-3-methylthiochroman-4-one(2.24 g, 6.823 mmol) prepared according to the known method in WO98/25916 was dissolved in dry tetrahydrofuran(30 ml) and then cooled to −78° C. Lithium aluminum hydride(1N solution in THF, 3.41 ml, 3.412 mmol) was added dropwise thereto and the resulting mixture was stirred overnight at room temperature. The reaction mixture was treated with saturated aqueous ammonium chloride solution(100 ml), extracted twice with ethyl acetate(100 ml), washed with water and saturated saline solution, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure and the residue was dissolved in 1,2-dichloroethane(30 ml). Zinc iodide(2.61 g, 8.188 mmol) and allyltrimethylsilane(2.17 ml, 13.646 mmol) were added dropwise thereto under cooling to 0° C. and the resulting mixture was stirred overnight at room temperature. The reaction mixture was diluted with water(200 ml), extracted twice with dichloromethane(200 ml), washed with water and saturated saline solution, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure and the residue thus obtained was purified by silica gel column chromatography(eluent:ethyl acetate/n-hexane=1/4, v/v) to give 1.4 g(Yield 58%) of the title compound.

後処理

  1. extractionextracted twice with ethyl acetate(100 ml)
  2. washwashed with water and saturated saline solution
  3. dry with materialdried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated under reduced pressure
  6. dissolutionthe residue was dissolved in 1,2-dichloroethane(30 ml)
  7. temperatureunder cooling to 0° C.
  8. stirringthe resulting mixture was stirred overnight at room temperature
  9. extractionextracted twice with dichloromethane(200 ml)
  10. washwashed with water and saturated saline solution
  11. dry with materialdried over anhydrous magnesium sulfate
  12. filtrationfiltered
  13. concentrationThe filtrate was concentrated under reduced pressure
  14. customthe residue thus obtained
  15. customwas purified by silica gel column chromatography(eluent

出典と根拠

ORDレコード
ord-d93885b9616f43f9a0be2a4248337d39
出典データセット
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06555571B2

反応ノート

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