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Potassium Hydroxide → 3-(Benzyloxy)-2-fluorobenzoic acid

HRID 2395386
ノート
印刷プレビュー

反応式

HRID 2395386 の反応式
[CH2:1]([O:8][C:9]1[C:10]([F:25])=[C:11]([CH:22]=[CH:23][CH:24]=1)[C:12]([O:14]CC1C=CC=CC=1)=[O:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[K+]>CO>[CH2:1]([O:8][C:9]1[C:10]([F:25])=[C:11]([CH:22]=[CH:23][CH:24]=1)[C:12]([OH:14])=[O:13])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH: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

4

反応物 2

HCID 14797Potassium HydroxideHCID 18971735HCID 18971735、化合物

生成物 1

HCID 189717253-(Benzyloxy)-2-fluorobenzoic acid収率 93.4%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of benzyl 3-benzyloxy-2-fluorobenzoate (7.13 g, 21 mmol) in methanol (40 ml) was added an aqueous solution of potassium hydroxide (2.38 g, 42 mmol in 40 ml of water) and the mixture heated at reflux for 30 min. The reaction mixture was cooled, washed with diethyl ether (20 ml) and the ethereal layer was discarded. The aqueous layer was acidified to pH 2 with concentrated HCl and extracted with ethyl acetate (3×40 ml). The combined organic extracts were washed with brine (20 ml), dried (MgSO4) and evaporated to afford title compound (4.83 g, 85%) as white solids.

後処理

  1. temperaturethe mixture heated
  2. temperatureat reflux for 30 min
  3. temperatureThe reaction mixture was cooled
  4. washwashed with diethyl ether (20 ml)
  5. extractionextracted with ethyl acetate (3×40 ml)
  6. washThe combined organic extracts were washed with brine (20 ml)
  7. dry with materialdried (MgSO4)
  8. customevaporated

出典と根拠

ORDレコード
ord-03c54bf9f22e49ff8651197cf2f710f8
出典データセット
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05814648

反応ノート

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