関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Lauric Acid | HCID 3893 | — |
| 反応物 | Lauryl alcohol diphosphonic acid | HCID 4395717 | — |
| 反応物 | HCID 20550621 | HCID 20550621 | — |
| 溶媒 | Phosphoric Acid | HCID 1004 | — |
| 溶媒 | Dibutyl butylphosphonate | HCID 6539 | — |
| 生成物 | Nonanoic Acid | HCID 8158 | — |
反応手順
In similar manner C9, C12, C16 and C18 extractants were prepared at 150° C. from iso-nonanoic, lauric, iso-hexadecanoic and stearic acids respectively. NMR analysis of the C12 extractant revealed that dodecane-1,1,2-triphosphonic acid was a major component of the crude product and that 1-hydroxy-1,1-dodecane diphosphonic acid was absent. When a solution of the crude C12 extractant (10 wt %) in dibutyl butylphosphonate (10 wt %) and kerosene (80 wt %) was shaken with equal volume of 10 M phosphoric acid, the total carbon in the phosphoric acid was 0.01%. The same amount of carbon was found when a 10 wt % kerosene solution of dibutyl butyl phosphonate was used instead. These results indicate that loss of material from the crude C12 extractant during contact with phosphoric acid is negligible. A C12 extractant was also made from lauric acid by reaction at 110° C. for 16 h. The main component of this acid extractant was 1-hydroxy-1,1 -dodecanediphosphonic acid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04316877 |
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| 出典データセット | uspto-grants-1982_02 |
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| ORD ID | ord-74634f1cc7ae49c980958fde48f33f85 |
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| 出典メモ | uspto-grants-1982_02 |
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