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Diethyl Ether → Stannane, (4-chlorophenyl)trimethyl-

HRID 535306
ノート
印刷プレビュー

反応式

HRID 535306 の反応式
[CH3:1][Sn:2](Cl)([CH3:4])[CH3:3].C1COCC1.[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([Mg]Br)=[CH:14][CH:13]=1.CCOCC>>[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([Sn:2]([CH3:4])([CH3:3])[CH3:1])=[CH:14][CH:13]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 3283Diethyl EtherHCID 8028TetrahydrofuranHCID 14016Trimethyltin chlorideHCID 178478191HCID 178478191、化合物

生成物 1

HCID 139674Stannane, (4-chlorophenyl)trimethyl-収率 97%

実験手順

To a 1M solution of trimethyltin chloride in THF (92 ml, 92 mmol) was slowly added a 1M solution of 4-chlorophenylmagnesium bromide in Et2O (92 ml, 92 mmol) over a 40 min period at −10° C. so that the temperature never exceed 0° C. After the addition, the cooling bath was removed and the resulting suspension was stirred at RT for 1 h. A saturated aqueous solution of NH4Cl (14 ml) was added followed by water until complete dissolution of the precipitate. The mixture was transferred into a separating funnel and extracted with Et2O (3×). The combined organic fractions were dried over Na2SO4, filtered and evaporated to dryness. The resulting crude material was purified by Combi-Flash Companion™ (Isco Inc.) column chromatography (SiO2; isocratic elution with cyclohexane) to yield the title compound (24.47 g, 89 mmol, 97%) as a colorless oil.

後処理

  1. additionAfter the addition
  2. customthe cooling bath was removed
  3. additionA saturated aqueous solution of NH4Cl (14 ml) was added
  4. dissolutionfollowed by water until complete dissolution of the precipitate
  5. customThe mixture was transferred into a separating funnel
  6. extractionextracted with Et2O (3×)
  7. dry with materialThe combined organic fractions were dried over Na2SO4
  8. filtrationfiltered
  9. customevaporated to dryness
  10. customThe resulting crude material was purified by Combi-Flash Companion™ (Isco Inc.) column chromatography (SiO2; isocratic elution with cyclohexane)

出典と根拠

ORDレコード
ord-9ea1ad047e78491daff65ebf3aff10e4
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08859535B2

反応ノート

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