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Diisobutylaluminum hydride → {3-[2-(Methyloxy)ethyl]-1-naphthalenyl}methanol

HRID 337601
ノート
印刷プレビュー

反応式

HRID 337601 の反応式
[CH3:1][O:2][CH2:3][CH2:4][C:5]1[CH:6]=[C:7]([C:15](OC)=[O:16])[C:8]2[C:13]([CH:14]=1)=[CH:12][CH:11]=[CH:10][CH:9]=2.CC(C[AlH]CC(C)C)C>C1(C)C=CC=CC=1>[CH3:1][O:2][CH2:3][CH2:4][C:5]1[CH:6]=[C:7]([CH2:15][OH:16])[C:8]2[C:13]([CH:14]=1)=[CH:12][CH:11]=[CH:10][CH:9]=2
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 14487Diisobutylaluminum hydrideHCID 66896973Methyl 3-[2-(methyloxy)ethyl]-1-naphthalenecarboxylate

生成物 1

HCID 66895342{3-[2-(Methyloxy)ethyl]-1-naphthalenyl}methanol

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

Methyl 3-[2-(methyloxy)ethyl]-1-naphthalenecarboxylate (1 eq.) from the previous step was taken up in toluene (0.1 M). To this solution was then added DIBAl-H (1.5 M toluene solution, 2.4 eq.) and the resulting solution was vigorously stirred at RT for 4 h. The reaction mixture thus obtained was quenched with 1 N aq. HCl and extracted with ether. The combined organic extracts were washed further with water and brine, dried over Na2SO4 and filtered. Concentration of the filtrate in vacuo afforded the title compound as a colorless oil.

後処理

  1. customThe reaction mixture thus obtained
  2. customwas quenched with 1 N aq. HCl
  3. extractionextracted with ether
  4. washThe combined organic extracts were washed further with water and brine
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered

出典と根拠

ORDレコード
ord-349d526a99cd44dd8403205221475222
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08889714B2

反応ノート

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