Quinone → HCID 178443135, compound

HRID 1649856Notes

Reaction equation

HRID 1649856 reaction equation
[CH2:1]=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[C:13]=[O:14].C=C.C1(P(C2C=CC=CC=2)CCCP(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(=O)C=CC(=O)C=C1>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.CO>[C:13]=[O:14].[CH2:1]=[CH2:2].[CH2:1]=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]

Participants

8

Conditions

Temperature
65 °C

Procedure

A carbon monoxide/ethylene/1-dodecene terpolymer was prepared by charging 180 ml of methanol and 78 ml of 1-dodecene to a magnetically stirred autoclave of 300 ml capacity. After the contents of the autoclave had been heated to 65° C., a 1:1 carbon monoxide and ethylene mixture was introduced under pressure until a pressure of 55 bar was reached. A catalyst solution was then introduced comprising 18 ml of methanol, 0.03 mmol of palladium acetate, 0.06 mmol of copper para-tosylate, 0.036 mmol of 1,3-bis(diphenylphosphino)propane, and 0.3 mmol of 1,4-benzoquinone. The pressure in the autoclave was maintained by introducing additional amounts of the 1:1 carbon monoxide and ethylene mixture. After 3 hours the polymerization was terminated by cooling to room temperature and releasing pressure. The polymer was filtered, washed with methanol and dried at 70° C.

Workup

  1. temperatureThe pressure in the autoclave was maintained
  2. customAfter 3 hours the polymerization was terminated
  3. temperatureby cooling to room temperature
  4. filtrationThe polymer was filtered
  5. washwashed with methanol
  6. customdried at 70° C.

Sources & evidence

ORD record
ord-2dcf6ae365284643841cf4ccd7fa31f6
Source dataset
uspto-grants-1990_05
Patent number
US04921937

Reaction notes

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