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Hydrochloric Acid → 2-hydroxy-4-(2,2,3,3,3-pentafluoropropoxy)benzoic Acid

HRID 733289
ノート
印刷プレビュー

反応式

HRID 733289 の反応式
[OH:1][C:2]1[CH:11]=[C:10]([O:12][CH2:13][C:14]([F:20])([F:19])[C:15]([F:18])([F:17])[F:16])[CH:9]=[CH:8][C:3]=1[C:4]([O:6]C)=[O:5].[OH-].[K+].Cl>CO.O>[OH:1][C:2]1[CH:11]=[C:10]([O:12][CH2:13][C:14]([F:19])([F:20])[C:15]([F:16])([F:17])[F:18])[CH:9]=[CH:8][C:3]=1[C:4]([OH:6])=[O:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 313Hydrochloric AcidHCID 14797Potassium HydroxideHCID 10108798Methyl 2-hydroxy-4-(2,2,3,3,3-pentafluoropropoxy)benzoate

生成物 1

HCID 97958622-hydroxy-4-(2,2,3,3,3-pentafluoropropoxy)benzoic Acid収率 55%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962
Water
溶媒
2 回

実験手順

To a solution of methyl 2-hydroxy-4-(2,2,3,3,3-pentafluoropropoxy)benzoate (obtained in example 1) (0.72 g, 2.40 mmol) in MeOH (9.7 mL), KOH (0.51 g, 86%; 7.80 mmol) dissolved in H2O (3 mL) was added and the resulting mixture was refluxed for 4 hours. The mixture was allowed to cool and MeOH was evaporated. The residue thus obtained was treated with H2O (5 mL) and the resulting solution was acidified with 6 N HCl. The white solid formed was collected by filtration, washed with cold H2O and dried in vacuo, yielding the title compound (55% yield).

後処理

  1. additionwas added
  2. temperaturethe resulting mixture was refluxed for 4 hours
  3. temperatureto cool
  4. customMeOH was evaporated
  5. customThe residue thus obtained
  6. customThe white solid formed
  7. filtrationwas collected by filtration
  8. washwashed with cold H2O
  9. customdried in vacuo

出典と根拠

ORDレコード
ord-f1c78b66d88c45098f3614ed179d93a8
出典データセット
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07589125B2

反応ノート

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