1,3,5-Trichlorobenzene → HCID 67899299, compound

HRID 1722815Notes

Reaction equation

HRID 1722815 reaction equation
[K].[Na].[Cl-:3].[Mg+2:4].[Cl-].[Cl:6][C:7]1[CH:12]=[C:11](Cl)[CH:10]=[C:9]([Cl:14])[CH:8]=1>O1CCCC1.Cl[Ni](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[Cl-:6].[Mg+2:4].[Cl:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([Cl:14])[CH:8]=1.[Cl-:3]

Participants

7

Procedure

A mixture of 5 g of potassium and sodium alloy (56:44) and 8.89 g of anhydrous magnesium chloride in 200 ml tetrahydrofuran (THF) was stirred at room temperature for one hour before refluxing for two hours. After cooling to room temperature, 13.64 g of 1,3,5-trichlorobenzene in 50 ml of THF was added over 1.5 hours during which time the reaction temperature was maintained below 35° C. The solution was then stirred for 10 hours at room temperature after which 105 mg of bis(triphenylphosphine)nickel dichloride was added, and the resulting reaction mixture refluxed for 24 hours. Most of the THF was removed under reduced pressure and the polymer product precipitated by methanol addition. After two precipitations 5.60 g of polymer was obtained: Tg=236° C.; Mn=7560; Mn=17500; D=2.30.

Workup

  1. temperaturebefore refluxing for two hours
  2. temperatureAfter cooling to room temperature
  3. temperaturewas maintained below 35° C
  4. additionwas added
  5. customthe resulting reaction mixture
  6. temperaturerefluxed for 24 hours
  7. customMost of the THF was removed under reduced pressure
  8. customthe polymer product precipitated by methanol addition
  9. customAfter two precipitations 5.60 g of polymer
  10. customwas obtained

Sources & evidence

ORD record
ord-10a47beb11f14021bbb892a392a9eaa2
Source dataset
uspto-grants-1989_08
Patent number
US04857630

Reaction notes

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