Methanol → Boric acid, calcium salt

HRID 1768888ノート

反応式

HRID 1768888 の反応式
[OH-].[Ca+2:2].[OH-].[B:4]([OH:7])([OH:6])[OH:5].C1(C)C(C)=CC=CC=1.CO>CCCCCC>[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]

参加物

6

反応条件

温度
60 °C

実験手順

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.

後処理

  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
  8. customthe methanol, reaction water and xylene
  9. filtrationfiltered
  10. customto remove any residual solids present
  11. distillationthe hexane was distilled out

出典と根拠

ORDレコード
ord-d2eeecd8a0714dbbbb0a8a80d3ebabc8
出典データセット
uspto-grants-1995_01
特許番号
US05380508

反応ノート

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