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Sodium Hydroxide → (E)-4-(3,3,3-Trifluoroprop-1-enyl)-2-methoxybenzoic acid

HRID 2102912
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HRID 2102912 반응식
[F:1][C:2]([F:18])([F:17])/[CH:3]=[CH:4]/[C:5]1[CH:14]=[CH:13][C:8]([C:9]([O:11]C)=[O:10])=[C:7]([O:15][CH3:16])[CH:6]=1.[OH-].[Na+]>CO>[F:1][C:2]([F:17])([F:18])/[CH:3]=[CH:4]/[C:5]1[CH:14]=[CH:13][C:8]([C:9]([OH:11])=[O:10])=[C:7]([O:15][CH3:16])[CH:6]=1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 68702754(E)-methyl 4-(3,3,3-trifluoroprop-1-enyl)-2-methoxybenzoate

생성물 1

HCID 57804194(E)-4-(3,3,3-Trifluoroprop-1-enyl)-2-methoxybenzoic acid

시약·촉매·용매 1

HCID 887Methanol용매

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온도
65 °C

실험 절차

A mixture of (E)-methyl 4-(3,3,3-trifluoroprop-1-enyl)-2-methoxybenzoate (340 mg, 0.0013 mol), MeOH (20 mL), and 2 N aqueous NaOH solution (1.5 mL) was stirred at 65° C. overnight. The solvents were removed under reduced pressure and the residue was treated with water, acidified with 1N HCl to pH 2-3, and extracted with EtOAc (50 mL×3). The combined organic layers were washed with brine, dried (Na2SO4), filtered and concentrated under vacuum to give the product as a white solid. LC-MS: 2.59 min, 244.8 (M−1).

후처리

  1. customThe solvents were removed under reduced pressure
  2. additionthe residue was treated with water
  3. extractionextracted with EtOAc (50 mL×3)
  4. washThe combined organic layers were washed with brine
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-49f90e5dc9d74439a38b5181cb17ea77
출처 데이터셋
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07576099B2

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