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

HRID 920738
ノート
印刷プレビュー

反応式

HRID 920738 の反応式
[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
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 962WaterHCID 14798Sodium HydroxideHCID 118062437Ethyl 1-((difluoromethoxy)methyl)cyclobutanecarboxylate

生成物 1

HCID 1180628681-((Difluoromethoxy)methyl)cyclobutanecarboxylic acid収率 35.2%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 8028Tetrahydrofuran
溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-a2ae08625a4948018e24eb7b47615d95
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09273058B2

反応ノート

読み込み中…

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