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Trimethyltin chloride → HCID 23070264、化合物

HRID 351300
ノート
印刷プレビュー

反応式

HRID 351300 の反応式
[S:1]1[C:5]2[S:6][CH:7]=[CH:8][C:4]=2[CH:3]=[CH:2]1.C([Li])CCC.[CH3:14][Sn:15](Cl)([CH3:17])[CH3:16]>C1COCC1>[CH3:14][Sn:15]([CH3:17])([CH3:16])[C:7]1[S:6][C:5]2[S:1][C:2]([Sn:15]([CH3:17])([CH3:16])[CH3:14])=[CH:3][C:4]=2[CH:8]=1
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

5

反応物 3

HCID 14016Trimethyltin chlorideHCID 136062Thieno(2,3-b)thiopheneHCID 178418339Butyllithium

生成物 1

HCID 23070264HCID 23070264、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-78 °C

実験手順

A solution of thieno[2,3-b]thiophene (2.81 g, 20 mmol) was dissolved in anhydrous THF (100 ml) and cooled to −78° C. under nitrogen. A solution of n-butyllithium (17.6 ml of a 2.5M solution in hexanes, 44 mmol) was added dropwise over 15 min, and the resulting solution was allowed to warm to RT and stirred at that temperature for 16 h. The resulting suspension was cooled to −78° C. and trimethyltin chloride (10.0 g, 50 mmol) was added at once as a solid. The reaction was allowed to warm to RT over 4 h and stirred at that temperature for an additional 20 h. The reaction was quenched by the addition of saturated sodium hydrogen carbonate (100 ml). Ethyl acetate (50 ml) was added and the layers separated. The organic layer was washed-with sodium carbonate (80 ml of a 2M aqeous solution) and brine (80 ml), dried (sodium sulfate), filtered and concentrated under reduced pressure. The resulting crude product was dry loaded onto a 20 g reverse phase silica column and eluted with acetonitrile. The first fraction was collected, concentrated and recrystallised from acetonitrile to afford the product as white flakes (4.15 g, 45%). M/Z cluster centred at 466 (M+). Found C, 31.1; H, 4.4; S,13.8, Calc. for C12H20S2Sn2 C, 30.9; H, 4.3; S, 13.8. 1H NMR (300 MHz, CDCl3) δ 7.23 (s, 2H), 0.38 (s,18H). 13C NMR (75 MHz, CDCl3) δ 152.4, 147.7, 142.7, 126.3, −8.2.

後処理

  1. temperatureto warm to RT
  2. temperatureThe resulting suspension was cooled to −78° C.
  3. temperatureto warm to RT over 4 h
  4. stirringstirred at that temperature for an additional 20 h
  5. customThe reaction was quenched by the addition of saturated sodium hydrogen carbonate (100 ml)
  6. additionEthyl acetate (50 ml) was added
  7. customthe layers separated
  8. dry with materialdried (sodium sulfate)
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure
  11. dry with materialThe resulting crude product was dry
  12. washeluted with acetonitrile
  13. customThe first fraction was collected
  14. concentrationconcentrated
  15. customrecrystallised from acetonitrile
  16. customto afford the product as white flakes (4.15 g, 45%)

出典と根拠

ORDレコード
ord-efffd494b2a94cde9c4394bfebcc9608
出典データセット
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07183418B2

反応ノート

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