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Glycerol → 7-Fluoroquinolin-8-ol

HRID 573972
ノート
印刷プレビュー

反応式

HRID 573972 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[OH:9].S(=O)(=O)(O)O.O[CH2:16][CH:17]([CH2:19]O)O>[N+](C1C=CC=CC=1)([O-])=O>[F:8][C:4]1[C:3]([OH:9])=[C:2]2[C:7]([CH:16]=[CH:17][CH:19]=[N:1]2)=[CH:6][CH:5]=1
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

5

反応物 3

HCID 753GlycerolHCID 1118Sulfuric AcidHCID 6435622-Amino-6-fluorophenol

生成物 1

HCID 218230207-Fluoroquinolin-8-ol収率 51.8%

試薬・触媒・溶媒 1

HCID 7416Nitrobenzene溶媒

反応条件

温度
140 °C

実験手順

To a solution of 2-amino-6-fluorophenol (4.0 g, 31.6 mmol) and nitrobenzene (20 mL) in a sealable reaction vessel was added in portions sulfuric acid (4.0 mL). Glycerol (12.0 g, 126 mmol) was added in one portion, and the solution turned to dark brown. The vessel was flushed with nitrogen, sealed and heated to 140° C. for 6 h. The reaction mixture was cooled to rt, diluted with 30 mL ice/water mixture, and washed 3 times with methyl t-butyl ether (removes most of the nitrobenzene). The aqueous phase was neutralized to pH=6-7 by slow addition of 6N NaOH. The resulting black precipitate was collected and the water solution was extracted with ethyl acetate 3 times. The organic extracts were combined with the black precipitate, concentrated in vacuo, and purified on silica gel column with 0-10% MeOH/DCM to give 2.67 g (51.7%) of 7-fluoro-8-quinolinol as an off-white solid.

後処理

  1. customThe vessel was flushed with nitrogen
  2. customsealed
  3. temperatureThe reaction mixture was cooled to rt
  4. additiondiluted with 30 mL ice/water mixture
  5. washwashed 3 times with methyl t-butyl ether (
  6. customremoves most of the nitrobenzene)
  7. additionThe aqueous phase was neutralized to pH=6-7 by slow addition of 6N NaOH
  8. customThe resulting black precipitate was collected
  9. extractionthe water solution was extracted with ethyl acetate 3 times
  10. concentrationconcentrated in vacuo
  11. custompurified on silica gel column with 0-10% MeOH/DCM

出典と根拠

ORDレコード
ord-b0c9b934a8274be9883aa0226e1caf1c
出典データセット
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09034303B2

反応ノート

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