Toluene → HCID 70505806, compound

HRID 1903896Notes

Reaction equation

HRID 1903896 reaction equation
[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]

Participants

6

Procedure

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.

Workup

  1. additionthe temperature of the mixture being kept below 45° during the addition
  2. filtrationwas filtered

Sources & evidence

ORD record
ord-75069aff937a48da8f0601c1984f8276
Source dataset
uspto-grants-1984_03
Patent number
US04439291

Reaction notes

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