Peracetic Acid → 4-(2,3-Epoxypropyl)-2,6-diphenylphenyl glycidyl ether

HRID 4149ノート

反応式

HRID 4149 の反応式
[CH2:1]([O:5][C:6]1[C:11]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:10][C:9]([CH2:18][CH:19]=[CH2:20])=[CH:8][C:7]=1[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[CH:2]1[O:4][CH2:3]1.C(OO)(=[O:29])C>C1(C)C=CC=CC=1.C([O-])(=O)C.[Na+]>[CH2:1]([O:5][C:6]1[C:7]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[CH:8][C:9]([CH2:18][CH:19]2[O:29][CH2:20]2)=[CH:10][C:11]=1[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH:2]1[O:4][CH2:3]1

参加物

5

実験手順

A 100 ml sulfurating flask equipped with stirrer, cooler, thermometer and drip funnel is charged with 13.7 g (0.04 mole) of 4-allyl-2,6-diphenylphenyl glycidyl ether in 20 ml of toluene and 0.7 g of sodium acetate. Over 2 hours, 9.13 g (0.048 mole) of 40% peracetic acid are added at a temperature in the range from 30° to 50° C. When the dropwise addition is complete, the reaction mixture is stirred for a further 7 hours. When the reaction is complete, the reaction mixture is diluted with 700 ml of toluene, the resultant aqueous phase is separated and the organic phase is washed with two 150 ml portions of NaHCO3 (5%) and then washed with 150 ml of water. The organic phase is dried over Na2SO4 and made peroxide-free with Na2SO3 and filtered. The filtrate is concentrated, affording 12.46 g (86.5%) of a yellow resin with an epoxide content of 4.99 eq/kg (89.5%) and a viscosity of 6850 mPas/40° C.

後処理

  1. customequipped with stirrer
  2. additionWhen the dropwise addition
  3. customthe resultant aqueous phase is separated
  4. washthe organic phase is washed with two 150 ml portions of NaHCO3 (5%)
  5. washwashed with 150 ml of water
  6. dry with materialThe organic phase is dried over Na2SO4
  7. filtrationfiltered
  8. concentrationThe filtrate is concentrated

出典と根拠

ORDレコード
ord-a11e6358c0444cb68a62cdc6256a2d8a
出典データセット
uspto-grants-1988_02
特許番号
US04724031

反応ノート

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