Azobisisobutyronitrile → 2-(3-(Bromomethyl)-5-methylphenyl)acetic acid

HRID 446401

反応式

HRID 446401 の反応式
C1C(=O)N([Br:8])C(=O)C1.[CH3:9][C:10]1[CH:11]=[C:12]([CH2:17][C:18]([OH:20])=[O:19])[CH:13]=[C:14]([CH3:16])[CH:15]=1.CC(N=NC(C#N)(C)C)(C#N)C>C(OCC)(=O)C>[Br:8][CH2:9][C:10]1[CH:11]=[C:12]([CH2:17][C:18]([OH:20])=[O:19])[CH:13]=[C:14]([CH3:16])[CH:15]=1

参加物

5

反応物 3

HCID 6547Azobisisobutyronitrile2 回HCID 67184N-bromobutanimideHCID 47494952-(3,5-Dimethylphenyl)acetic acid

生成物 1

HCID 581686112-(3-(Bromomethyl)-5-methylphenyl)acetic acid

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

NBS (3.12 g) was added portionwise over 1 hour to a solution of 2-(3,5-dimethylphenyl)acetic acid (3.6 g) and AIBN (0.015 g) in ethyl acetate (100 mL) at 50° C. under nitrogen. More AIBN (0.015 g) was added and the mixture was heated to reflux for 3 hours. The reaction mixture was washed with 10% aqueous sodium chloride solution (2×200 mL), dried over magnesium sulphate, filtered and evaporated. The crude material was purified by flash silica chromatography using 20% ethyl acetate in isohexane containing 1% acetic acid as solvent. Fractions containing the product were evaporated to dryness to afford a solid which was triturated with cyclohexane (10 mL) to yield the subtitled compound as a white solid. Yield 2.10 g.

後処理

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 3 hours
  3. washThe reaction mixture was washed with 10% aqueous sodium chloride solution (2×200 mL)
  4. dry with materialdried over magnesium sulphate
  5. filtrationfiltered
  6. customevaporated
  7. customThe crude material was purified by flash silica chromatography
  8. additionFractions containing the product
  9. customwere evaporated to dryness
  10. customto afford a solid which
  11. customwas triturated with cyclohexane (10 mL)

出典と根拠

ORDレコード
ord-f2447fa1d584478fb82909664d6f56d8
出典データセット
uspto-grants-2013_07
特許番号
US08476265B2

関連ノート

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