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Potassium Hydroxide → 2,3-Diphenyl-2-cyclopropene-1-carboxylic acid

HRID 1740064
ノート
印刷プレビュー

反応式

HRID 1740064 の反応式
[C:1]1([C:7]2[CH:8]([C:16]([O:18]CC)=[O:17])[C:9]=2[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[K+]>CO>[C:10]1([C:9]2[CH:8]([C:16]([OH:18])=[O:17])[C:7]=2[C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 14797Potassium HydroxideHCID 281943Ethyl 2,3-diphenylcycloprop-2-ene-1-carboxylate

生成物 1

HCID 3473832,3-Diphenyl-2-cyclopropene-1-carboxylic acid収率 78%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Ethyl 2,3-diphenyl-cycloprop-2-ene-1-carboxylate (1.75 g, 6.6 mol) and potassium hydroxide (1.79 g, 31.9 mmol) were dissolved in methanol (60 cm3) and heated to reflux for 5 hours. The mixture was cooled to room temperature and the solvent evaporated. The residue was partitioned between water (30 cm3) and ethyl acetate (30 cm3) The aqueous layer was separated and washed with ethyl acetate (2×30 cm3) before being acidified to pH=1 with dilute hydrochloric acid and extracted with dichloromethane (3×40 cm3). The combined dichloromethane extracts were dried (MgSO4) and evaporated to give the cyclopropene acid 1.22 g, 78%.

後処理

  1. temperatureheated
  2. temperatureto reflux for 5 hours
  3. customthe solvent evaporated
  4. customThe residue was partitioned between water (30 cm3) and ethyl acetate (30 cm3) The aqueous layer
  5. customwas separated
  6. washwashed with ethyl acetate (2×30 cm3)
  7. extractionextracted with dichloromethane (3×40 cm3)
  8. dry with materialThe combined dichloromethane extracts were dried (MgSO4)
  9. customevaporated

出典と根拠

ORDレコード
ord-b717bd3b0e1c41278b5b4c639d257024
出典データセット
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05968968

反応ノート

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