Toluene → HCID 70505806、化合物
反応式
[Na][Na].[CH2:3]([C:6]1[CH:7]=[C:8]([C:13]([C:16]2[CH:21]=[CH:20][C:19]([OH:22])=[C:18]([CH2:23][CH:24]=[CH2:25])[CH:17]=2)([CH3:15])[CH3:14])[CH:9]=[CH:10][C:11]=1[OH:12])[CH:4]=[CH2:5].C(C1[C:35]([OH:36])=[C:34]([C:37]([CH3:40])(C)C)C=C(C)C=1)(C)(C)C.[C:42](Cl)(=[O:46])[C:43](C)=[CH2:44].[C:48]1(C)C=CC=CC=1>>[CH2:23]([C:18]1[CH:17]=[C:16]([C:13]([C:8]2[CH:9]=[CH:10][C:11]([O:12][C:35](=[O:36])[CH:34]=[CH:37][CH3:40])=[C:6]([CH2:3][CH:4]=[CH2:5])[CH:7]=2)([CH3:15])[CH3:14])[CH:21]=[CH:20][C:19]=1[O:22][C:42](=[O:46])[CH:43]=[CH:44][CH3:48])[CH:24]=[CH2:25]参加物
6
実験手順
To a stirred mixture of 68.5 g of the disodium salt of 2,2-bis(3-allyl-4-hydroxyphenyl)propane, 250 ml of toluene, and 0.12 g of 2,6-di-tert. butyl-p-cresol was added dropwise over 1 hour 40.3 g of methacryloyl chloride, the temperature of the mixture being kept below 45° during the addition. After the mixture had been stirred for a further 21/2 hours, it was filtered and the filtrate was freed of solvent by subjecting it to vacuum (water pump) and then high vacuum. There remained in practically quantitative yield the desired product, having theformula ##STR18##as a nearly colourless liquid of viscosity 3.6 Pa-s.
後処理
- additionthe temperature of the mixture being kept below 45° during the addition
- filtrationwas filtered
出典と根拠
- ORDレコード
- ord-75069aff937a48da8f0601c1984f8276
- 出典データセット
- uspto-grants-1984_03
- 特許番号
- US04439291
反応ノート
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