Tetrahydrofuran → HCID 86682691、化合物

HRID 449788

反応式

HRID 449788 の反応式
[O:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.[CH:6]1([C:12]2[CH:18]=[CH:17][C:15]([OH:16])=[CH:14][C:13]=2[OH:19])[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1.[H-].[Na+].[P:22](Cl)([O:32][CH2:33][C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1)([O:24][CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)=[O:23]>O>[CH2:5]([O:1][P:22]([O:16][C:15]1[CH:17]=[CH:18][C:12]([CH:6]2[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11]2)=[C:13]([O:19][P:22]([O:32][CH2:33][C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)([O:24][CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)=[O:23])[CH:14]=1)([O:24][CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)=[O:23])[C:4]1[CH:33]=[CH:34][CH:35]=[CH:2][CH:3]=1

参加物

6

反応条件

温度
0 °C

実験手順

To a tetrahydrofuran solution (10 ml) of 4-cyclohexylresorcinol (926 mg), sodium hydride (60% dispersion in liquid paraffin) (404 mg) was added and stirred at 0° C. for 30 minutes. Then, dibenzyl chlorophosphate (10 w/v % solution in benzene) (30 ml) was added dropwise. After stirring at room temperature for 3 hours, water (30 ml) was added to the reaction mixture, and the extraction was carried out with ethyl acetate (30 ml). Then, the extract was washed with saturated brine (20 ml), dried with anhydrous sodium sulfate and then concentrated. The residue (4.12 g) was subjected to silica gel chromatography (silica gel 90 g, chloroform to chloroform:methanol=100:1), to give 1,3-bis(dibenzylphosphonooxy)-4-cyclohexylbenzene (2.19 g, yield: 64%) as a yellow liquid.

後処理

  1. stirringAfter stirring at room temperature for 3 hours
  2. extractionthe extraction
  3. washThen, the extract was washed with saturated brine (20 ml)
  4. dry with materialdried with anhydrous sodium sulfate
  5. concentrationconcentrated

出典と根拠

ORDレコード
ord-e3fe8978e03448e5b19ee71f2e107697
出典データセット
uspto-grants-2013_07
特許番号
US08486919B2

関連ノート

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