Styrene → HCID 86738954, compound

HRID 463788Notes

Reaction equation

HRID 463788 reaction equation
C(=O)(O)[O-].[Na+].[H+].[H+].Cl[Pt-2:9](Cl)(Cl)(Cl)(Cl)Cl.[CH2:15]=[CH:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.[Pt]>C(O)C>[Pt:9].[CH2:15]=[CH:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

Participants

6

Conditions

Temperature
55 °C

Procedure

The platinum-styrene complex used in the following examples is prepared by adding 6 parts of sodium bicarbonate to a mixture containing 3 parts of chloroplatinic acid (H2PtCl6.6H2O), 6 parts of styrene and 50 parts of ethanol. The mixture is heated to reflux temperature (about 55° C.), and then refluxed for about 35 minutes with agitation, and then cooled to room temperature. The resultant mixture is filtered and the crystals thus obtained washed with about 30 parts of acetone. After adding about 30 parts of xylene to the filtrate, orange crystals are formed. These crystals are filtered, recovered and dried. The crystals are dissolved in sufficient isopropanol to form a solution containing 0.75 percent by weight of elemental platinum.

Workup

  1. customis prepared
  2. temperatureThe mixture is heated
  3. temperaturerefluxed for about 35 minutes with agitation
  4. temperaturecooled to room temperature
  5. filtrationThe resultant mixture is filtered
  6. customthe crystals thus obtained
  7. washwashed with about 30 parts of acetone
  8. additionAfter adding about 30 parts of xylene to the filtrate, orange crystals
  9. customare formed
  10. filtrationThese crystals are filtered
  11. customrecovered
  12. customdried
  13. dissolutionThe crystals are dissolved in sufficient isopropanol
  14. customto form a solution

Sources & evidence

ORD record
ord-fc38c16ad1bc487ca02739825033a350
Source dataset
uspto-grants-1985_10
Patent number
US04544696

Reaction notes

Loading…