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Borane → 3-Iodo-4-methylbenzyl alcohol

HRID 375467
ノート
印刷プレビュー

反応式

HRID 375467 の反応式
[I:1][C:2]1[C:10](C)=CC=C[C:3]=1[C:4](O)=O.B.[O:13]1[CH2:17][CH2:16][CH2:15][CH2:14]1>>[I:1][C:2]1[CH:10]=[C:16]([CH2:17][OH:13])[CH:15]=[CH:14][C:3]=1[CH3:4]
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 3

HCID 6331BoraneHCID 8028Tetrahydrofuran2 回HCID 27593652-Iodo-3-methylbenzoic acid

生成物 1

HCID 51667983-Iodo-4-methylbenzyl alcohol

実験手順

To a solution of 5.0 g (19.1 mmol) of 2-iodo-3-methyl benzoic acid in 50 mL of anhydrous tetrahydrofuran, was slowly added 22 mL of a 1M borane solution in tetrahydrofuran. The resultant reaction mixture was reacted for approximately ninety minutes and then was quenched with ethanol resulting in the evolution of hydrogen gas. The mixture was diluted with ethyl acetate. The resulting layers were separated and the organic layer was washed sequentially with sodium bicarbonate and brine, dried over sodium sulfate, filtered and crystallized from a hexane/ethyl acetate mixture to provide 120 mg of the desired subtitled compound.

後処理

  1. customThe resultant reaction mixture
  2. customwas reacted for approximately ninety minutes
  3. customwas quenched with ethanol resulting in the evolution of hydrogen gas
  4. additionThe mixture was diluted with ethyl acetate
  5. customThe resulting layers were separated
  6. washthe organic layer was washed sequentially with sodium bicarbonate and brine
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. customcrystallized from a hexane/ethyl acetate mixture

出典と根拠

ORDレコード
ord-ce5abc58716640fcab829b36fc17100b
出典データセット
uspto-grants-1996_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05484926

反応ノート

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