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Water → 1-((Difluoromethoxy)methyl)cyclobutanecarboxylic acid

HRID 920738
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HRID 920738 반응식
[F:1][CH:2]([F:14])[O:3][CH2:4][C:5]1([C:9]([O:11]CC)=[O:10])[CH2:8][CH2:7][CH2:6]1.O.[OH-].[Na+]>C(O)C.C1COCC1>[F:1][CH:2]([F:14])[O:3][CH2:4][C:5]1([C:9]([OH:11])=[O:10])[CH2:8][CH2:7][CH2:6]1
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참가 물질

6

반응물 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 118062437Ethyl 1-((difluoromethoxy)methyl)cyclobutanecarboxylate

생성물 1

HCID 1180628681-((Difluoromethoxy)methyl)cyclobutanecarboxylic acid수율 35.2%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 8028Tetrahydrofuran
용매

실험 절차

To a stirred solution of Intermediate 223A (0.263 g, 1.263 mmol) in ethanol (3.5 mL), THF (3.5 mL), and water (3 mL) was added NaOH (0.152 g, 3.79 mmol) and the reaction mixture was stirred at RT for 16 h. The reaction mixture was concentrated and the residue dissolved in water and extracted with ethyl acetate (3×15 mL) The aqueous layer was then acidified to pH 2-3 using a 1.5 N aqueous solution of HCl and extracted with EtOAc (3×15 mL). The combined organic layer was washed with water, dried over Na2SO4 and concentrated to afford Intermediate 223B as a brown oil (0.08 g, 35% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 12.41 (s, 1H), 6.97-6.40 (m, 1H), 4.15-3.90 (m, 2H), 2.38-2.09 (m, 2H), 2.01-1.51 (m, 4H).

후처리

  1. concentrationThe reaction mixture was concentrated
  2. dissolutionthe residue dissolved in water
  3. extractionextracted with ethyl acetate (3×15 mL) The aqueous layer
  4. extractionextracted with EtOAc (3×15 mL)
  5. washThe combined organic layer was washed with water
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-a2ae08625a4948018e24eb7b47615d95
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09273058B2

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