3-Hydroxybenzoic Acid → HCID 15225618、化合物

HRID 1770128ノート

反応式

HRID 1770128 の反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6].[CH:11]1([CH:17]([CH:19]2[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]2)O)[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N(C(OCC)=O)=NC(OCC)=O>O.O1CCOCC1>[CH:11]1([CH:17]([CH:19]2[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24]2)[O:1][C:2]2[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=2)[C:5]([OH:7])=[O:6])[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1

参加物

7

実験手順

To a solution of 3-hydroxybenzoic acid (1.61 g, 8.2 mmol), dicyclohexylmethanol (1.61 g, 8.2 mmol), triphenylphosphine (2.05 g, 7.82 mmol) and dioxane (35 ml) was added diethyl azodicarboxylate (1.41 ml, 8.94 mmol), and the resultant mixture was refluxed for 3 days. The reaction mixture was allowed to warm up to room temperature, poured into chilled water and extracted with diethyl ether. The organic layer was concentrated, and the residue was dissolved in a mixture of methanol (20 ml), tetrahydrofuran (6.5 ml) and water (2.0 ml), mixed with potassium hydroxide (1.16 g) and stirred for 2 hours. The mixture was poured into chilled water, acidified, and extracted with ethyl acetate. The organic layer was concentrated, and the resultant residue was recrystallized from hexane to give the titled compound (0.43 g, yield 18%).

後処理

  1. additionpoured
  2. extractionextracted with diethyl ether
  3. concentrationThe organic layer was concentrated
  4. dissolutionthe residue was dissolved in a mixture of methanol (20 ml), tetrahydrofuran (6.5 ml) and water (2.0 ml)
  5. additionmixed with potassium hydroxide (1.16 g)
  6. additionThe mixture was poured
  7. temperatureinto chilled water
  8. extractionextracted with ethyl acetate
  9. concentrationThe organic layer was concentrated
  10. customthe resultant residue was recrystallized from hexane

出典と根拠

ORDレコード
ord-d90969d5d77d4293bc01a73a9a256904
出典データセット
uspto-grants-1995_01
特許番号
US05385917

反応ノート

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