Ethanol → 2-(4-Tert-butylphenoxy)acetic acid

HRID 280248

反応式

HRID 280248 の反応式
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([OH:11])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].C(O)C.C[O-].[Na+].Br[CH2:19][C:20]([OH:22])=[O:21]>CO.Cl>[C:1]([C:5]1[CH:6]=[CH:7][C:8]([O:11][CH2:19][C:20]([OH:22])=[O:21])=[CH:9][CH:10]=1)([CH3:4])([CH3:2])[CH3:3]

参加物

7

実験手順

4-t-butylphenol, 37.5 gm, was added to 300 ml of ethanol. 57.2 gm of a 25% solution of sodium methoxide (2equivalents) in methanol was then added to the system. The system was stirred at room temperature for approximately 0.5 hour. Afterwards, 29.5 ml of bromoacetic acid was added and the system was then heated to reflux for 18 hours. The reaction was then stopped and the solvent removed by stripping. The resulting solid was dissolved in methylene chloride; dilute sodium hydroxide was added to give a basic pH. The resulting precipitate was dissolved in hydrochloric acid and then extracted with methylene chloride. The methylene chloride was then stripped, and the resulting crude product air dried. Toluene was then added to the product. The toluene was removed by stripping and any remaining water was azeotroped off with the toluene to give 33.3 gm of 4-t-butylphenoxyacetic acid.

後処理

  1. temperaturethe system was then heated
  2. temperatureto reflux for 18 hours
  3. customthe solvent removed by stripping
  4. dissolutionThe resulting solid was dissolved in methylene chloride
  5. additiondilute sodium hydroxide was added
  6. customto give a basic pH
  7. extractionextracted with methylene chloride
  8. dry with materialthe resulting crude product air dried
  9. additionToluene was then added to the product
  10. customThe toluene was removed
  11. customany remaining water was azeotroped off with the toluene

出典と根拠

ORDレコード
ord-82708de6621e427e870f49da4368c195
出典データセット
uspto-grants-1986_05
特許番号
US04588735

関連ノート

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