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

HRID 733289
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HRID 733289 반응식
[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]
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참가 물질

6

반응물 3

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

생성물 1

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

시약·촉매·용매 2

HCID 887Methanol용매HCID 962
Water
용매
2회

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-f1c78b66d88c45098f3614ed179d93a8
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07589125B2

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