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Potassium tert-butoxide → HCID 86700852、化合物

HRID 881749
ノート
印刷プレビュー

反応式

HRID 881749 の反応式
[Cl-].[CH3:2][O:3][CH3:4].[C:5]1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CC(C)([O-])C.[K+].[Br:30][CH:31]1[C:36]2([C:39]3[CH:44]=[CH:43][C:42]([Cl:45])=[CH:41][CH:40]=3)[CH2:37][CH2:38][C:33](C=O)([CH2:34][O:35]2)[CH2:32]1>O1CCCC1>[Br:30][CH:31]1[C:36]2([C:39]3[CH:44]=[CH:43][C:42]([Cl:45])=[CH:41][CH:40]=3)[CH2:37][CH2:38][C:33]([CH:5]=[CH:2][O:3][CH3:4])([CH2:34][O:35]2)[CH2:32]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 3

HCID 23665647Potassium tert-butoxideHCID 86700850HCID 86700850、化合物HCID 86700853HCID 86700853、化合物

生成物 1

HCID 86700852HCID 86700852、化合物収率 95%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a solution of triphenylphosphine methoxymethane chloride (3.51 g, 10.24 mmol) in tetrahydrofuran (20 ml) under nitrogen at room temperature, was added potassium t-butoxide (1.149 g, 10.24 mmol). The reddish solution was stirred at room temperature for 90 minutes. Then a solution of 6-bromo-1-(4-chloro-phenyl)-2-oxa-bicyclo[2.2.2]octane-4-carbaldehyde (2.25 g, 6.83 mmol) in tetrahydrofuran (6 ml) was added to the reaction mixture. The reaction mixture was stirred at room temperature for 10 minutes and then quenched with water (2 ml). The mixture was partitioned between brine (15 ml) and ethyl acetate (60 ml). The aqueous layer was extracted with ethyl acetate (2×30 ml) and the combined organic extracts were washed with brine, dried over Na2SO4, and concentrated. The residue was purified by flash chromatography (heptanes/acetone 2/1) to afford the cis and trans mixtures of 6-bromo-1-(4-chloro-phenyl)-4-(2-methoxy-vinyl)-2-oxa-bicyclo[2.2.2]octane (2.32 g, 95%) as colorless oil. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.74-2.99 (m, 6H) 3.54 (3.89 (m, 4H) 3.91-6.36 (m, 5H) 7.28-7.43 (m, 4H).

後処理

  1. stirringThe reaction mixture was stirred at room temperature for 10 minutes
  2. customquenched with water (2 ml)
  3. customThe mixture was partitioned between brine (15 ml) and ethyl acetate (60 ml)
  4. extractionThe aqueous layer was extracted with ethyl acetate (2×30 ml)
  5. washthe combined organic extracts were washed with brine
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated
  8. customThe residue was purified by flash chromatography (heptanes/acetone 2/1)

出典と根拠

ORDレコード
ord-42920343c21b4535bc1decb24c3dacf7
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08993619B2

反応ノート

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