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Acetic Acid → HCID 68698458、化合物

HRID 1990845
ノート
印刷プレビュー

反応式

HRID 1990845 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:9]2[O:13][CH2:12][CH2:11][O:10]2)[CH:5]=[C:6](Br)[CH:7]=1.[Li]CCCC.B(OC)(OC)[O:20]C.C(O)(=O)C.OO.O>C1COCC1>[Br:1][C:2]1[CH:7]=[C:6]([OH:20])[CH:5]=[C:4]([CH:9]2[O:13][CH2:12][CH2:11][O:10]2)[CH:3]=1
参加物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 176Acetic AcidHCID 784Hydrogen PeroxideHCID 962WaterHCID 8470Trimethyl borateHCID 11301269HCID 11301269、化合物HCID 178418339Butyllithium

生成物 1

HCID 68698458HCID 68698458、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 2-(3,5-dibromo-phenyl)-[1,3]dioxolane (20.25 g, 65.75 mmol, 1.0 equiv) in anhydrous THF (200 mL) was added n-BuLi (45.2 mL, 72.33 mmol, 1.1 equiv, 1.6 M solution in hexane) at −78° C. under Ar. After stirring the reaction mixture for 30 min, trimethyl borate (7.33 mL, 6.83 g, 65.75 mmol, 1.0 equiv) was added rapidly and the reaction allowed to come to 0° C. over a time period of 4 h. A solution of conc. acetic acid (5.64 mL, 5.92 g, 98.63 mmol, 1.5 equiv) was slowly added followed by addition of a solution of 35% hydrogen peroxide in water (6.3 mL, 7.03 g, 72.33 mmol, 1.1 equiv) and the reaction mixture kept at 0° C. for 30 min. After stirring at rt for an additional 4 h, the reaction was extracted with ethyl actetate (3×200 mL), the combined organic phases washed with water, dried over MgSO4 and concentrated by evaporation under reduced pressure. The title compound was obtained in quantitative yield (16.1 g). MS (EI): 245.0 [M]+.

後処理

  1. customto come to 0° C. over a time period of 4 h
  2. waitthe reaction mixture kept at 0° C. for 30 min
  3. stirringAfter stirring at rt for an additional 4 h
  4. extractionthe reaction was extracted with ethyl actetate (3×200 mL)
  5. washthe combined organic phases washed with water
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated by evaporation under reduced pressure

出典と根拠

ORDレコード
ord-7bc93ff1c7bb47efb80f7fea177269d8
出典データセット
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07645753B2

反応ノート

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