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Potassium Carbonate → 2-Chloro-5-(4-fluoro-benzyloxy)-quinoline

HRID 2076278
ノート
印刷プレビュー

反応式

HRID 2076278 の反応式
[OH:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6]([Cl:12])=[N:7]2.C(=O)([O-])[O-].[K+].[K+].[F:19][C:20]1[CH:27]=[CH:26][C:23]([CH2:24]Br)=[CH:22][CH:21]=1>CC(C)=O>[Cl:12][C:6]1[CH:5]=[CH:4][C:3]2[C:8](=[CH:9][CH:10]=[CH:11][C:2]=2[O:1][CH2:24][C:23]2[CH:26]=[CH:27][C:20]([F:19])=[CH:21][CH:22]=2)[N:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 11430Potassium CarbonateHCID 680214-Fluorobenzyl bromideHCID 1354422212-chloroquinolin-5-ol

生成物 1

HCID 866194962-Chloro-5-(4-fluoro-benzyloxy)-quinoline収率 48.7%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

5-Hydroxy-2-chloroquinoline (CAS 124467-35-2, 0.6 g, 3.0 mmol) was dissolved in 15 mL acetone and potassium carbonate (555 mg, 3.0 mmol) was added. Then 4-fluoro-benzylbromide (0.5 ml, 4.0 mmol) was added and the reaction mixture stirred for 18 hours at ambient temperature. The mixture was evaporated and the residue taken up in water and extracted (3×) with ethyl acetate. The combined organic phases were dried over sodium sulfate and evaporated. The residue was subjected to flash column chromatography on silica gel (heptane/ethyl acetate 90:10->80:20 gradient) to yield 2-chloro-5-(4-fluoro-benzyloxy)-quinoline as a white solid (420 mg, 44%), MS: m/e=289 (M+H+).

後処理

  1. customThe mixture was evaporated
  2. extractionextracted (3×) with ethyl acetate
  3. dry with materialThe combined organic phases were dried over sodium sulfate
  4. customevaporated

出典と根拠

ORDレコード
ord-65cc4096bb694fec8ec3c8ce96e5a2f2
出典データセット
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07923561B2

反応ノート

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