Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Boric Acid | HCID 7628 | — |
| Reactant | Calcium Hydroxide | HCID 6093208 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Boric acid, calcium salt | HCID 134660 | — |
Reaction Steps
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 120 g of methanol, 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 methanol, reaction 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. However, the thus obtained calcium borate overbased alkylsalicylate caused its gelation and was found generally unusable as an additive for petroleum products.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05380508 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-d2eeecd8a0714dbbbb0a8a80d3ebabc8 |
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| Source note | uspto-grants-1995_01 |
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