Morpholine → Chroman-2-ol

HRID 1030820

反応式

HRID 1030820 の反応式
C(C1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH:7]=[CH:6][C:5]=1[OH:14])(=O)C.C1C2CC(=[O:22])C(C2)C1.N1CCOCC1>C1(C)C=CC=CC=1>[O:22]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH2:7][CH2:6][CH:5]1[OH:14]

参加物

5

反応物 3

HCID 8083MorpholineHCID 10345Bicyclo(2.2.1)heptan-2-oneHCID 684551-(2-Hydroxy-1-naphthyl)ethan-1-one

生成物 1

HCID 11171070Chroman-2-ol

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

A solution was prepared by dissolving 10 g (0.054 mole) of 1-acetyl-2-naphthol, 6.6 g (0.06 mole) of norcamphor and 8.7 g (0.10 mole) of morpholine in 300 cc of toluene, and the solution was boiled for 5 hours and water was separated. After termination of the reaction. toluene was removed under reduced pressure, and the remaining chromanone compound was recrystallized from acetone, and the chromanon compound was dissolved in 200 cc of methanol and lithium aluminum hydride was added to the solution to form a chromanol compound. Then, 6.49 g of this chromanol compound was heated at 170° C. to 180° C. together with anhydrous copper sulfate in a carbon dioxide current for 10 minutes and the obtained brown viscous liquid was purified by the chromatography on silica gel to obtain 5.1 g of a chromene compound represented by the following formula: ##STR71##

後処理

  1. customA solution was prepared
  2. customwater was separated
  3. customAfter termination of the reaction
  4. customtoluene was removed under reduced pressure
  5. customthe remaining chromanone compound was recrystallized from acetone
  6. dissolutionthe chromanon compound was dissolved in 200 cc of methanol
  7. additionlithium aluminum hydride was added to the solution

出典と根拠

ORDレコード
ord-5e633be37a594465a20e146efac7179e
出典データセット
uspto-grants-1992_04
特許番号
US05106998

関連ノート

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