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Carbon Dioxide → 4-(Trimethylsilyl)benzoic acid

HRID 1969117
ノート
印刷プレビュー

反応式

HRID 1969117 の反応式
Br[C:2]1[CH:7]=[CH:6][C:5]([Si:8]([CH3:11])([CH3:10])[CH3:9])=[CH:4][CH:3]=1.C([Li])CCC.[C:17](=[O:19])=[O:18]>C1COCC1>[CH3:9][Si:8]([CH3:11])([CH3:10])[C:5]1[CH:6]=[CH:7][C:2]([C:17]([OH:19])=[O:18])=[CH:3][CH:4]=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 280Carbon Dioxide2 回HCID 138897Silane, (4-bromophenyl)trimethyl-HCID 178418339Butyllithium

生成物 1

HCID 2801694-(Trimethylsilyl)benzoic acid

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-78 °C

実験手順

To 1-bromo-4-(trimethylsilyl)-benzene (Aldrich) (6.42 g, 28.04 mmol) in a clean, dry 250 mL round-bottom flask was added THF (100 mL) and the mixture was cooled to −78° C. with stirring for 10 minutes under nitrogen. Then, a 2.5M solution of n-butyllithium in hexanes (13.46 mL, 1.2 eq) was added slowly over about seven minutes. The resulting mixture was stirred at −78° C. for 1.5 hours (solution turned light yellow). Then, at −78° C. an excess of dry ice (4 large pieces) were added to the reaction mixture (solution turned color, then became clear) and the dry ice bath was removed and stirred for 15 minutes. TLC confirmed that the reaction was complete, and after stirring an additional 10 minutes at −78° C., the reaction was quenched with water (100 mL). Ethyl acetate (500 mL) was then added and with stirring 4N HCl was added to pH=2. The layers were separated and then washed the ethyl acetate layer with brine (1×250 mL) and finally the organic layer was dried over magnesium sulfate, filtered, concentrated and pumped to give 4-Trimethylsilanyl-benzoic acid as a white solid (5.49 g).

後処理

  1. stirringThe resulting mixture was stirred at −78° C. for 1.5 hours (solution turned light yellow)
  2. customwas removed
  3. stirringstirred for 15 minutes
  4. stirringafter stirring an additional 10 minutes at −78° C.
  5. customthe reaction was quenched with water (100 mL)
  6. additionEthyl acetate (500 mL) was then added
  7. stirringwith stirring 4N HCl
  8. additionwas added to pH=2
  9. customThe layers were separated
  10. washwashed the ethyl acetate layer with brine (1×250 mL)
  11. dry with materialfinally the organic layer was dried over magnesium sulfate
  12. filtrationfiltered
  13. concentrationconcentrated

出典と根拠

ORDレコード
ord-b159a70c922f41808e3447fa8f3ce53f
出典データセット
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08426441B2

反応ノート

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