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Tributylstannane → (2E,4E)-5-(tri-n-butylstannyl)-3-methylpenta-2,4-dien-1-ol

HRID 567955
ノート
印刷プレビュー

反応式

HRID 567955 の反応式
C([Cu])#N.C([Li])CCC.[SnH:9]([CH2:18][CH2:19][CH2:20][CH3:21])([CH2:14][CH2:15][CH2:16][CH3:17])[CH2:10][CH2:11][CH2:12][CH3:13].[H][H].[CH3:24]/[C:25](/[C:29]#[CH:30])=[CH:26]\[CH2:27][OH:28].[NH4+].[OH-].[NH4+].[Cl-]>C1COCC1>[CH2:18]([Sn:9]([CH2:10][CH2:11][CH2:12][CH3:13])([CH2:14][CH2:15][CH2:16][CH3:17])/[CH:30]=[CH:29]/[C:25](/[CH3:24])=[CH:26]/[CH2:27][OH:28])[CH2:19][CH2:20][CH3:21]
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

8

反応物 6

HCID 5948TributylstannaneHCID 53676041-Pentol, (E)-HCID 21863491Ammonium chloride ammonium hydroxideHCID 178418339ButyllithiumHCID 178418361HCID 178418361、化合物HCID 178418546HCID 178418546、化合物

生成物 1

HCID 10992697
(2E,4E)-5-(tri-n-butylstannyl)-3-methylpenta-2,4-dien-1-ol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-78 °C

実験手順

CuCN (2.01 g, 22.40 mmol) is introduced into a round-bottomed flask placed under argon, THF (60 ml) is then added and the mixture is cooled to −78° C. n-Butyl-lithium (1.6M, 27.7 ml, 44.40 mmol) is then added dropwise and the mixture is allowed to slowly return to room temperature. It is again cooled to −78° C. and n-Bu3SnH (12 ml, 44.40 mmol) is added and the mixture is stirred for 10 minutes, during which the hydrogen is discharged. (2E)-3-Methylpent-2-en-4-yn-1-ol (1.86 g, 19.31 mmol) is then added, the reaction mixture is left stirring for 45 minutes and then poured into 200 ml of an NH4OH/NH4Cl (10/90) solution. Extraction is carried out with ether (3×100 ml), drying is carried out over Na2SO4 and evaporation is carried out under vacuum.

後処理

  1. additionis then added dropwise
  2. customto slowly return to room temperature
  3. waitthe reaction mixture is left
  4. extractionExtraction
  5. customdrying
  6. customis carried out over Na2SO4 and evaporation

出典と根拠

ORDレコード
ord-3706d33b26a64329a2c5fc71af18e273
出典データセット
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06180674B2

反応ノート

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