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Ethyl fluoroacetate → 1-(5-Bromo-2-fluorophenyl)-2-fluoroethanone

HRID 627635
ノート
印刷プレビュー

反応式

HRID 627635 の反応式
[Li+].CC([N-]C(C)C)C.CCCCCCC.C1COCC1.C(C1C=CC=CC=1)C.[Br:29][C:30]1[CH:35]=[CH:34][C:33]([F:36])=[CH:32][CH:31]=1.[F:37][CH2:38][C:39](OCC)=[O:40]>C1COCC1>[Br:29][C:30]1[CH:35]=[CH:34][C:33]([F:36])=[C:32]([C:39](=[O:40])[CH2:38][F:37])[CH:31]=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

6

反応物 4

HCID 9988Ethyl fluoroacetateHCID 99931-Bromo-4-fluorobenzeneHCID 2724682Lithium diisopropylamideHCID 22742125Tetrahydrofuran heptane ethylbenzol

生成物 1

HCID 867157171-(5-Bromo-2-fluorophenyl)-2-fluoroethanone収率 28.4%

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
-78 °C

実験手順

A 2.0 M solution of LDA in heptane/THF/ethylbenzene (100 mL, 200 mmol) was added dropwise via syringe to a solution of 1-bromo-4-fluorobenzene (20 mL, 182 mmol) in THF (600 mL) at −78° C. After stirring for 2.5 hours at −78° C., ethyl monofluoroacetate (18.47 mL, 191 mmol) was added dropwise via syringe, and the reaction was stirred at −78° C. for 20 minutes and then stirred at −45° C. for 30 minutes before being quenched with saturated aqueous ammonium chloride at −45° C. The mixture was diluted with water and ethyl acetate. The layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic extracts were washed with saturated aqueous ammonium chloride, water, and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated. The crude product was dissolved in a minimal amount of methanol and placed in a −20° C. freezer overnight. The resulting solid was collected and washed with cold methanol to afford the title intermediate (12.07 g, 51.6 mmol, 28% yield) as a white solid.

後処理

  1. stirringthe reaction was stirred at −78° C. for 20 minutes
  2. stirringstirred at −45° C. for 30 minutes
  3. custombefore being quenched with saturated aqueous ammonium chloride at −45° C
  4. additionThe mixture was diluted with water and ethyl acetate
  5. customThe layers were separated
  6. extractionthe aqueous layer was extracted with ethyl acetate
  7. washThe combined organic extracts were washed with saturated aqueous ammonium chloride, water, and saturated aqueous sodium chloride
  8. dry with materialdried over anhydrous magnesium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated
  11. dissolutionThe crude product was dissolved in a minimal amount of methanol
  12. waitplaced in a −20° C. freezer overnight
  13. customThe resulting solid was collected
  14. washwashed with cold methanol

出典と根拠

ORDレコード
ord-90cdd91fd6f140b0ad607f52051758cf
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09309263B2

反応ノート

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