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2,2-Difluoro-2-(fluorosulfonyl)acetic acid → Ethyl 1-((difluoromethoxy)methyl)cyclobutanecarboxylate

HRID 920737
ノート
印刷プレビュー

反応式

HRID 920737 の反応式
[OH:1][CH2:2][C:3]1([C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH2:6][CH2:5][CH2:4]1.[F:12][C:13]([F:21])(S(F)(=O)=O)C(O)=O>C(#N)C.[Cu]I>[F:12][CH:13]([F:21])[O:1][CH2:2][C:3]1([C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH2:6][CH2:5][CH2:4]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 27375162,2-Difluoro-2-(fluorosulfonyl)acetic acidHCID 15670506Ethyl 1-(hydroxymethyl)cyclobutane-1-carboxylate

生成物 1

HCID 118062437Ethyl 1-((difluoromethoxy)methyl)cyclobutanecarboxylate収率 76%

試薬・触媒・溶媒 2

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)触媒HCID 6342Acetonitrile溶媒

反応条件

温度
50 °C

実験手順

To a stirred solution of ethyl 1-(hydroxymethyl)cyclobutanecarboxylate (0.2 g, 1.264 mmol) in acetonitrile (2 mL) was added CuI (0.120 g, 0.632 mmol) and the reaction mass was heated to 50° C. 2,2-Difluoro-2-(fluorosulfonyl)acetic acid (0.196 mL, 1.896 mmol) added dropwise to the solution and the reaction mixture was stirred at 50° C. for 4 h. The reaction mixture was cooled to RT and extracted with EtOAc (3×15 mL). The combined organic layer was washed with a 10% aqueous solution of NaHCO3, dried over Na2SO4, filtered and the filtrate concentrated to afford Intermediate 223A as a brown oil (0.2 g, 76%). 1H NMR (300 MHz, DMSO-d6) δ ppm 6.94-6.39 (m, 1H), 4.16-3.99 (m, 4H), 2.41-2.17 (m, 2H), 2.08-1.73 (m, 4H), 1.26-1.09 (m, 3H).

後処理

  1. temperatureThe reaction mixture was cooled to RT
  2. extractionextracted with EtOAc (3×15 mL)
  3. washThe combined organic layer was washed with a 10% aqueous solution of NaHCO3
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationthe filtrate concentrated

出典と根拠

ORDレコード
ord-42822d8344754ca3be083fce78d0b132
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

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