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2-t-Butyl-5-[(E)-2-ethoxycarbonylethenyl]-1-nitrobenzene → 2-t-Butyl-5-[(1E)-3-hydroxy-1-propenyl]-1-nitrobenzene

HRID 1637497
ノート
印刷プレビュー

反応式

HRID 1637497 の反応式
[C:1]([C:5]1[CH:10]=[CH:9][C:8](/[CH:11]=[CH:12]/[C:13](OCC)=[O:14])=[CH:7][C:6]=1[N+:18]([O-:20])=[O:19])([CH3:4])([CH3:3])[CH3:2].[H-].C([Al+]CC(C)C)C(C)C>O1CCCC1>[C:1]([C:5]1[CH:10]=[CH:9][C:8](/[CH:11]=[CH:12]/[CH2:13][OH:14])=[CH:7][C:6]=1[N+:18]([O-:20])=[O:19])([CH3:4])([CH3:2])[CH3:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 193484662-t-Butyl-5-[(E)-2-ethoxycarbonylethenyl]-1-nitrobenzeneHCID 21225700Diisobutylaluminumhydride

生成物 1

HCID 193484672-t-Butyl-5-[(1E)-3-hydroxy-1-propenyl]-1-nitrobenzene収率 90%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of 9.24 g (33.4 mmol) of 2-t-butyl-5-[(E)-2-ethoxycarbonylethenyl]-1-nitrobenzene [prepared as described in step (ii) above] in 200 ml of tetrahydrofuran was cooled to -70° C. in a dry ice-acetone bath, and 100 ml (100 mmol) of a 1 M solution of diisobutylaluminum hydride in tetrahydrofuran were added dropwise thereto over a period of 45 minutes. The resulting mixture was then stirred for a further 30 minutes. At the end of this time, the reaction temperature was allowed to rise to 0° C., and the reaction was quenched by adding dropwise a mixture of 4 ml of methanol and 20 ml of tetrahydrofuran. The reaction mixture was then poured into 2 N aqueous hydrochloric acid-ice, after which it was extracted with ethyl acetate. The extract was washed with water and with a saturated aqueous solution of sodium chloride, in that order, after which it was dried over anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure, and the resulting residue was purified by column chromatography through 300 g of silica gel, using a 2:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 7.06 g (yield 90%) of the title compound as an oily substance.

後処理

  1. customto rise to 0° C.
  2. customthe reaction was quenched
  3. additionby adding dropwise
  4. additiona mixture of 4 ml of methanol and 20 ml of tetrahydrofuran
  5. additionThe reaction mixture was then poured into 2 N aqueous hydrochloric acid-ice
  6. extractionafter which it was extracted with ethyl acetate
  7. washThe extract was washed with water and with a saturated aqueous solution of sodium chloride, in that order
  8. dry with materialafter which it was dried over anhydrous sodium sulfate
  9. customThe solvent was removed by distillation under reduced pressure
  10. customthe resulting residue was purified by column chromatography through 300 g of silica gel
  11. additionby volume mixture of hexane and ethyl acetate as the eluent

出典と根拠

ORDレコード
ord-8d1c628074984bc89c7079a086b072e7
出典データセット
uspto-grants-2000_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06040339

反応ノート

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