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Tetrahydrofuran → 2-Ethyl-8-methoxyquinoline-5-carboxylic acid

HRID 2393087
ノート
印刷プレビュー

反応式

HRID 2393087 の反応式
Br[C:2]1[CH:11]=[CH:10][C:9]([O:12][CH3:13])=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6]([CH2:14][CH3:15])=[N:7]2.[OH-:16].[Na+].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[C]=O.[O:39]1[CH2:43]CCC1>O.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.Cl[Pd]Cl>[CH2:14]([C:6]1[CH:5]=[CH:4][C:3]2[C:2]([C:43]([OH:39])=[O:16])=[CH:11][CH:10]=[C:9]([O:12][CH3:13])[C:8]=2[N:7]=1)[CH3:15]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 8028TetrahydrofuranHCID 11776TriphenylphosphineHCID 14798Sodium HydroxideHCID 18979097HCID 18979097、化合物HCID 178418416HCID 178418416、化合物

生成物 1

HCID 189790842-Ethyl-8-methoxyquinoline-5-carboxylic acid

試薬・触媒・溶媒 2

HCID 6102075
Dichlorobis(triphenylphosphine)palladium
触媒
HCID 962Water溶媒

反応条件

温度
105 °C

実験手順

A mixture of 5-bromo-2-ethyl-8-methoxyquinoline (3.3 g), sodium hydroxide (3.1 g, 46% solution in water), triphenylphosphine (0.22 g), and bis(triphenylphosphine)palladium (II) chloride (0.14 g) in tetrahydrofuran (14 ml) and water (7 ml) was stirred in a pressurised reaction vessel and charged with carbon monoxide to a pressure of 160 psi. The vessel was heated to 105° C. and stirred for 24 hours. The reaction was allowed to cool and depressurised. The mixture was filtered and the solid collected washed with tetrahydrofuran (2×10 ml). The solid was dissolved in hot methanol (10 ml) and water (10 ml), and the solution filtered to remove any remaining solids. The hot solution was treated with glacial acetic acid (2 ml) and cooled in ice. The resulting precipitate was filtered off and dried over silica gel under vacuum to afford the title compound as a white solid (0.44 g).

後処理

  1. stirringstirred for 24 hours
  2. temperatureto cool
  3. filtrationThe mixture was filtered
  4. customthe solid collected
  5. washwashed with tetrahydrofuran (2×10 ml)
  6. dissolutionThe solid was dissolved in hot methanol (10 ml)
  7. filtrationwater (10 ml), and the solution filtered
  8. customto remove any remaining solids
  9. additionThe hot solution was treated with glacial acetic acid (2 ml)
  10. temperaturecooled in ice
  11. filtrationThe resulting precipitate was filtered off
  12. customdried over silica gel under vacuum

出典と根拠

ORDレコード
ord-a097b292da0942bc9f65e885f774f466
出典データセット
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05804588

反応ノート

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