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

HRID 337601
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HRID 337601 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14487Diisobutylaluminum hydrideHCID 66896973Methyl 3-[2-(methyloxy)ethyl]-1-naphthalenecarboxylate

생성물 1

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

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-349d526a99cd44dd8403205221475222
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08889714B2

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