p-Toluenesulfonic acid monohydrate → tetrahydro-3-hexyl-4-hydroxy-(R)-6-undecyl-2H-pyran-2-one

HRID 703683ノート

反応式

HRID 703683 の反応式
[CH2:1]([C@H:7]([CH:11]([OH:32])[CH2:12][CH:13](OC1CCCCO1)[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[C:8](O)=[O:9])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[OH2:33].C1(C)C=CC(S(O)(=O)=O)=CC=1>C(O)C>[CH2:1]([C@@H:7]1[CH:11]([OH:32])[CH2:12][CH:13]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[O:33][C:8]1=[O:9])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6]

参加物

4

反応物 2

HCID 521998p-Toluenesulfonic acid monohydrateHCID 678557542-hexyl-3-hydroxy-(R)-5-[(tetrahydro-2H-pyran-2-yl)oxy]hexadecanoic acid

生成物 1

HCID 67855756tetrahydro-3-hexyl-4-hydroxy-(R)-6-undecyl-2H-pyran-2-one

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

15.4 g of a diastereomer mixture of 2-hexyl-3-hydroxy-(R)-5 [(tetrahydro-2H -pyran-2-yl)oxy]hexadecanoic acid are dissolved in 160 ml of ethanol and 800 mg of toluene-4-sulphonic acid monohydrate are added. The reaction mixture is heated to 55°-60° C. until the reaction has finished. The solvent is removed in vacuo and the residue is dissolved in 160 ml of dichloromethane. The solution is stirred at room temperature for 1 hour. The reaction mixture is evaporated. The material obtained is chromatographed on silica gel. There is obtained tetrahydro-3-hexyl-4-hydroxy-(R)-6-undecyl-2H-pyran-2-one, m.p. 95°-96° C.

後処理

  1. temperatureThe reaction mixture is heated to 55°-60° C. until the reaction
  2. customThe solvent is removed in vacuo
  3. dissolutionthe residue is dissolved in 160 ml of dichloromethane
  4. customThe reaction mixture is evaporated
  5. customThe material obtained
  6. customis chromatographed on silica gel

出典と根拠

ORDレコード
ord-01d7d0a81f374c4f888157fbe69620a6
出典データセット
uspto-grants-1991_01
特許番号
US04983746

反応ノート

読み込み中…