Water → 1-(4-Pyridyl)-2,3-bis(hydroxymethyl)-6,7-dimethoxynaphthalene

HRID 1743030

반응식

HRID 1743030 반응식
[N:1]1[CH:6]=[CH:5][C:4]([C:7]2[C:16]3[C:11](=[CH:12][C:13]([O:19][CH3:20])=[C:14]([O:17][CH3:18])[CH:15]=3)[CH:10]=[C:9]([C:21](OC)=[O:22])[C:8]=2[C:25](OC)=[O:26])=[CH:3][CH:2]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>O1CCCC1>[N:1]1[CH:6]=[CH:5][C:4]([C:7]2[C:16]3[C:11](=[CH:12][C:13]([O:19][CH3:20])=[C:14]([O:17][CH3:18])[CH:15]=3)[CH:10]=[C:9]([CH2:21][OH:22])[C:8]=2[CH2:25][OH:26])=[CH:3][CH:2]=1

참가 물질

6

반응물 4

HCID 962Water2회HCID 14798Sodium HydroxideHCID 117286421-(4-Pyridyl)-2,3-bis(methoxycarbonyl)-6,7-dimethoxynaphthaleneHCID 21226445Aluminium lithium hydride

생성물 1

HCID 220074131-(4-Pyridyl)-2,3-bis(hydroxymethyl)-6,7-dimethoxynaphthalene수율 80%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of 1-(4-pyridyl)-2,3-bis(methoxycarbonyl)-6,7-dimethoxynaphthalene (2.0 g) in tetrahydrofuran (50 ml) is added dropwise to a suspension of lithium aluminum hydride (100 mg) in tetrahydrofuran (20 ml) at -20° C. The mixture is stirred under ice-cooling for one hour, and thereto are added water (0.1 ml) and 15% aqueous sodium hydroxide solution (0.1 ml). Ten minutes thereafter, water (0.3 ml) is added to the reaction mixture, and the mixture is stirred at room temperature for one hour. The insoluble materials are removed by filtration on celite, and the filtrate is concentrated. The residue is recrystallized from a mixture of ethyl acetate and diethyl ether (1:1) to give 1-(4-pyridyl)-2,3-bis(hydroxymethyl)-6,7-dimethoxynaphthalene (1.35 g).

후처리

  1. temperaturecooling for one hour
  2. stirringthe mixture is stirred at room temperature for one hour
  3. customThe insoluble materials are removed by filtration on celite
  4. concentrationthe filtrate is concentrated
  5. customThe residue is recrystallized from a mixture of ethyl acetate and diethyl ether (1:1)

출처 및 근거

ORD 기록
ord-a8ca16ee622e4d3780416f0149f58f03
출처 데이터셋
uspto-grants-1994_08
특허 번호
US05342941

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