O-Xylene → Boric acid, calcium salt

HRID 1768887Notes

Reaction equation

HRID 1768887 reaction equation
[OH-].[Ca+2:2].[OH-].[B:4]([OH:7])([OH:6])[OH:5].C1(C)C(C)=CC=CC=1>O>[B:4]([O-:7])([O-:6])[O-:5].[Ca+2:2].[B:4]([O-:7])([O-:6])[O-:5].[Ca+2:2].[Ca+2:2]

Participants

5

Conditions

Temperature
60 °C

Procedure

200 g of the same neutral calcium alkylsalicylate (A) as used in Example 1, 26 g of calcium hydroxide (B), 43.4 g (2.0 moles per mole of the calcium hydroxide) of orthoboric acid (C) and 400 g of xylene (F) were put in a 1000-ml four-necked flask fitted with a condenser and heated to 60° C. while agitating. To this mixture was added 20 g of water, and the resulting mixture was heated up to a refluxing temperature (66° C.) under agitation and reacted for 4 hours to obtain a reaction product. The reaction product was further heated to 140° C. for 1.5 hours to distill out the water and xylene. Finally the reaction product was diluted twofold with hexane and filtered to remove any residual solids present, and the hexane was distilled out to obtain a calcium borate overbased alkylsalicylate.

Workup

  1. customwere put in a 1000-ml four-necked flask
  2. customfitted with a condenser
  3. temperaturethe resulting mixture was heated up to a refluxing temperature (66° C.) under agitation
  4. customreacted for 4 hours
  5. customto obtain a reaction product
  6. temperatureThe reaction product was further heated to 140° C. for 1.5 hours
  7. distillationto distill out the water and xylene
  8. additionFinally the reaction product was diluted twofold with hexane
  9. filtrationfiltered
  10. customto remove any residual solids present
  11. distillationthe hexane was distilled out

Sources & evidence

ORD record
ord-8da2f68ee808453cb98e6a2dd422600a
Source dataset
uspto-grants-1995_01
Patent number
US05380508

Reaction notes

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