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Acetic Acid → 2-(4-Bromo-3-fluorophenyl)pyrrolidine

HRID 415152
ノート
印刷プレビュー

反応式

HRID 415152 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH2:9][CH2:10][CH2:11][N:12]=2)=[CH:4][C:3]=1[F:13].[BH3-]C#N.[Na+].C(O)(=O)C>CO>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:9][CH2:10][CH2:11][NH:12]2)=[CH:4][C:3]=1[F:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 176Acetic AcidHCID 5003444Sodium cyanoborohydrideHCID 666213385-(4-bromo-3-fluorophenyl)-3,4-dihydro-2H-pyrrole

生成物 1

HCID 534036242-(4-Bromo-3-fluorophenyl)pyrrolidine収率 98%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of 5-(4-bromo-3-fluorophenyl)-3,4-dihydro-2H-pyrrole ((12.7 g, 52.7 mmol) in 360 mL methanol was added NaBH3CN (6.6 g, 105 mmol) at 0° C. The resulting solution was adjusted to pH=6 with acetic acid. The reaction mixture was stirred at room temperature overnight. The reaction was quenched with 2 N HCl and the methanol was removed by evaporation. The residue was diluted with water, the aqueous phase adjusted to pH=10 with NaOH, extracted with ethyl acetate, dried by Na2SO4, concentrated and the residue was purified by chromatography on silica gel to give 2-(4-bromo-3-fluorophenyl)pyrrolidine as a yellow solid (12.5 g, yield 98%). LC-MS (ESI) m/z: 244 (M+1)+.

後処理

  1. customThe reaction was quenched with 2 N HCl
  2. customthe methanol was removed by evaporation
  3. additionThe residue was diluted with water
  4. extractionextracted with ethyl acetate
  5. dry with materialdried by Na2SO4
  6. concentrationconcentrated
  7. customthe residue was purified by chromatography on silica gel

出典と根拠

ORDレコード
ord-90e9127cecf34070a4e5dca854305378
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08088760B2

反応ノート

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