Ethyl 4-iodobenzoate → Ethyl 4-(3,3-difluorocyclobutanecarbonyl)benzoate

HRID 537488ノート

反応式

HRID 537488 の反応式
I[C:2]1[CH:12]=[CH:11][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:4][CH:3]=1.[F:13][C:14]1([F:21])[CH2:17][CH:16]([C:18](Cl)=[O:19])[CH2:15]1>O1CCCC1.Cl.[Cu](I)I>[F:13][C:14]1([F:21])[CH2:17][CH:16]([C:18]([C:2]2[CH:12]=[CH:11][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:4][CH:3]=2)=[O:19])[CH2:15]1

参加物

6

反応物 2

HCID 142891Ethyl 4-iodobenzoateHCID 838550033,3-Difluorocyclobutanecarbonyl chloride

生成物 1

HCID 68157446Ethyl 4-(3,3-difluorocyclobutanecarbonyl)benzoate収率 16%

試薬・触媒・溶媒 3

HCID 83717Copper iodide触媒HCID 313Hydrochloric Acid溶媒HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

In a 3-neck flask at −30° C. containing ethyl 4-iodobenzoate (600 mg, 2.17 mmol) in anhydrous tetrahydrofuran (6.00 mL) was added isopropylmagnesium chloride lithium chloride complex (1.84 mL, 2.39 mmol) dropwise and then stirred at the same temperature for another 40 min. Copper iodide (124 mg, 0.650 mmol) was then added quickly in one portion. The mixture was brought to −15° C. for 20 min. to ensure the solid has dissolved. The reaction is then brought back to −40° C. Crude 3,3-difluorocyclobutanecarbonyl chloride (470 mg, 1.50 mmol pure) was then added and the reaction was then warmed to 0° C. over 1 h and then stirred at room temperature for 18 h. The mixture was then diluted with 1 N HCl and extracted three times with ethyl acetate. The combined organic layers were then washed with brine and then dried over sodium sulfate, filtered, and concentrated to provide 680 mg of crude oil. Purification by silica gel flash chromatography (0-10% ethyl acetate in heptane) afforded impure ethyl 4-(3,3-difluorocyclobutanecarbonyl)benzoate (130 mg, approximately 0.24 mmol pure) as a solid. 1H NMR (400 MHz, CDCl3) δ 8.09 (d, J=9.0 Hz, 2H), 7.18 (d, J=9.2 Hz, 2H), 4.39 (q, J=7.4 Hz, 2H), 3.34-3.15 (m, 1H), 3.12-2.78 (m, 4H), 1.40 (t, J=7.4 Hz, 3H).

後処理

  1. additionwas added isopropylmagnesium chloride lithium chloride complex (1.84 mL, 2.39 mmol) dropwise
  2. waitThe mixture was brought to −15° C. for 20 min.
  3. dissolutionhas dissolved
  4. customis then brought back to −40° C
  5. stirringstirred at room temperature for 18 h
  6. extractionextracted three times with ethyl acetate
  7. washThe combined organic layers were then washed with brine
  8. dry with materialdried over sodium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customto provide 680 mg of crude oil
  12. customPurification by silica gel flash chromatography (0-10% ethyl acetate in heptane)

出典と根拠

ORDレコード
ord-9b23502cbc6f4ca496daf15a8de0a459
出典データセット
uspto-grants-2014_10
特許番号
US08859591B2

反応ノート

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