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Benzyl Bromide → Ethyl 1-benzyl-3-bromo-4-methyl-5-(trifluoromethyl)-1H-pyrrole-2-carboxylate

HRID 623779
ノート
印刷プレビュー

反応式

HRID 623779 の反応式
[CH2:1](Br)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Br:9][C:10]1[C:14]([CH3:15])=[C:13]([C:16]([F:19])([F:18])[F:17])[NH:12][C:11]=1[C:20]([O:22][CH2:23][CH3:24])=[O:21].C([O-])([O-])=O.[K+].[K+]>C(#N)C.CCOC(C)=O.O>[CH2:1]([N:12]1[C:13]([C:16]([F:19])([F:17])[F:18])=[C:14]([CH3:15])[C:10]([Br:9])=[C:11]1[C:20]([O:22][CH2:23][CH3:24])=[O:21])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=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

7

反応物 3

HCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 86711863Ethyl 3-bromo-4-methyl-5-(trifluoromethyl)-1H-pyrrole-2-carboxylate

生成物 1

HCID 86711864Ethyl 1-benzyl-3-bromo-4-methyl-5-(trifluoromethyl)-1H-pyrrole-2-carboxylate収率 89.2%

試薬・触媒・溶媒 3

HCID 962Water溶媒
HCID 6342
Acetonitrile
溶媒
HCID 8857Ethyl Acetate溶媒

反応条件

温度
80 °C

実験手順

Benzyl bromide (10.9 mL, 91.66 mmol) was added to the solution of crude ethyl 3-bromo-4-methyl-5-(trifluoromethyl)-1H-pyrrole-2-carboxylate (25 g, 83.33 mmol) and K2CO3 (23.03 g, 166.66 mmol) in acetonitrile. The reaction mixture was stirred for 13 h at 80° C. Then the reaction mixture was cooled to RT and then diluted with EtOAc and H2O. The aqueous layer was extracted with EtOAc (2×400 mL). Combined organic layer was dried over anhydrous Na2SO4, concentrated under reduced pressure to yield crude mass which was then purified by column chromatography (100-200 mesh Silica gel; 10% ethyl acetate/hexane; Rf-value 0.8) to afford title compound (29 g, 89.18% yield, pale yellow color oil).

後処理

  1. temperatureThen the reaction mixture was cooled to RT
  2. extractionThe aqueous layer was extracted with EtOAc (2×400 mL)
  3. dry with materialCombined organic layer was dried over anhydrous Na2SO4
  4. concentrationconcentrated under reduced pressure
  5. customto yield crude mass which
  6. customwas then purified by column chromatography (100-200 mesh Silica gel; 10% ethyl acetate/hexane; Rf-value 0.8)

出典と根拠

ORDレコード
ord-8b724a8843334160a54ac07f9bcc9f9f
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09302988B2

反応ノート

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