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Aluminium lithium hydride → (3-(Hydroxymethyl)-5-methoxyphenyl)methanol

HRID 2253724
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HRID 2253724 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:14]([O-])=[O:15])[CH:6]=[C:7]([CH:13]=1)[C:8](OCC)=[O:9].[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1.CCOCC>[OH:9][CH2:8][C:7]1[CH:13]=[C:3]([O:2][CH3:1])[CH:4]=[C:5]([CH2:14][OH:15])[CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 21226445Aluminium lithium hydrideHCID 86747067Methyl,methyl 5-methoxyisophthalate

생성물 1

HCID 4114928(3-(Hydroxymethyl)-5-methoxyphenyl)methanol

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 5.00 g (22.32 mmoles) of methyl,methyl 5-methoxyisophthalate in 100 ml dry THF is added dropwise, maintaining a gentle reflux, 67 ml (66.96 mmoles) of a 1M solution of lithium aluminum hydride in Et2O. After addition the reaction mixture is stirred for 1 hour and is then quenched with saturated NH4Cl. The reaction mixture is then extracted with Et2O (3 times). The Et2O layers are combined, washed with brine, dried with MgSO4, filtered and concentrated down in vacuo to yield 1,3-di-(hydroxymethyl)-5-methoxybenzene which is used directly in the next step.

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후처리

  1. additionAfter addition the reaction mixture
  2. customis then quenched with saturated NH4Cl
  3. extractionThe reaction mixture is then extracted with Et2O (3 times)
  4. washwashed with brine
  5. dry with materialdried with MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated down in vacuo

출처 및 근거

ORD 기록
ord-73af88ba3a93488ca2e5a9dc2d63d393
출처 데이터셋
uspto-grants-1993_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05232948

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