Toluene → HCID 86735486, compound

HRID 616712Notes

Reaction equation

HRID 616712 reaction equation
[C:1]([O-:6])(=[O:5])[C:2]([CH3:4])=[CH2:3].[CH2:7]([Sn+:11]([CH2:16][CH2:17][CH2:18][CH3:19])[CH2:12][CH2:13][CH2:14][CH3:15])[CH2:8][CH2:9][CH3:10].[C:20]1([CH3:26])[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>>[C:1]([O-:6])(=[O:5])[C:2]([CH3:4])=[CH2:3].[CH2:16]([Sn+:11]([CH2:7][CH2:8][CH2:9][CH3:10])[CH2:12][CH2:13][CH2:14][CH3:15])[CH2:17][CH2:18][CH3:19].[CH2:1]=[CH:26][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1

Participants

3

Procedure

S5 was synthesized by the general method described above. In this synthesis, equimolar quantities of tri-n-butyltin methacrylate (0.1 mole) and stryene (0.1 mole) were reacted with the azo initiator* in 85 ml of toluene for 96 hours. The resultant polymer was a transparent, orange tinted elastomer which could be cast as a film from the toluene solution. Analysis showed 20.90% Sn.

Workup

  1. customS5 was synthesized by the general method

Sources & evidence

ORD record
ord-c944a87b34b041febf6c1453fbaf7637
Source dataset
uspto-grants-1978_02
Patent number
US04075319

Reaction notes

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