Benzoyl Peroxide → 4-Cyano-3-fluorobenzyl bromide

HRID 277770

反応式

HRID 277770 の反応式
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH3:9])=[CH:5][C:4]=1[F:10])#[N:2].[Br:11]N1C(=O)CCC1=O.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>C(Cl)(Cl)(Cl)Cl>[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][Br:11])=[CH:5][C:4]=1[F:10])#[N:2]

参加物

5

反応物 3

HCID 7187Benzoyl PeroxideHCID 67184N-bromobutanimide2 回HCID 27784432-Fluoro-4-methylbenzonitrile

生成物 1

HCID 27784664-Cyano-3-fluorobenzyl bromide

試薬・触媒・溶媒 1

HCID 5943Carbon Tetrachloride溶媒

実験手順

To a solution of the product from Step C (22.2 g, 165 mmol) in 220 mL of carbontetrachloride was added N-bromosuccinimide (29.2 g, 164 mmol) and benzoylperoxide (1.1 g). The reaction was heated to reflux for 30 minutes, then cooled to room temperature. The solution was concentrated in vacuo to one-third the original volume, poured into EtOAc, washed with water, sat. aq. NaHCO3, and brine, then dried (Na2SO4), filtered, and concentrated in vacuo to provide the crude product. Analysis by 1H NMR indicated only partial conversion, so the crude material was resubjected to the same reaction conditions for 2.5 hours, using 18 g (102 mmol) of N-bromosuccinimide. After workup, the crude material was purified by silica gel chromatography (0-10% EtOAc/hexane) to provide the desired product.

後処理

  1. temperatureThe reaction was heated
  2. temperatureto reflux for 30 minutes
  3. concentrationThe solution was concentrated in vacuo to one-third the original volume
  4. additionpoured into EtOAc
  5. washwashed with water, sat. aq. NaHCO3, and brine
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customto provide the crude product
  10. customAfter workup, the crude material was purified by silica gel chromatography (0-10% EtOAc/hexane)

出典と根拠

ORDレコード
ord-ac1029f7e11d4135b78234ba2b4320ae
出典データセット
uspto-grants-2002_03
特許番号
US06358956B1

関連ノート

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