関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,2-Octadecanediol | HCID 89314 | — |
| 反応物 | Dimethyl ester phosphorous acid | HCID 94853 | — |
| 反応物 | 1,2-Hexadecanediol | HCID 98037 | — |
| 反応物 | Pentadecane-1,2-diol | HCID 118123 | — |
| 反応物 | 1,2-Heptadecanediol | HCID 3015706 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Pentadecanediol Octadecanediol | HCID 86740139 | — |
反応手順
Approximately 360 g of the 1,2-mixed pentadecanedioloctadecanediol (obtained from Viking Chemical Co. as Vikol 158 containing about 28% 1,2-pentadecanediol, about 28% 1,2-hexadecanediol, about 28% 1,2-heptadecanediol and about 16% 1,2-octadecanediol) were charged to a glass reactor equipped with heater, agitator, Dean-Stark tube with condenser and provision for blanketing the vapor space with nitrogen. The contents were heated to 70° C. to liquify and 55 g of dimethyl hydrogen phosphite were slowly added. The reaction mixture was heated to 110° C. and held for 2 hours, held at 120° C. for 1 hour, and held at 130° C. for 1 hour. During this reaction period, methanol distilled over and condensed into the trap. The crude product was vacuum stripped at 150° C. to remove volatile materials. 379 g of finished additive were produced. The product was an amber fluid which became waxy on cooling.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04532057 |
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| 出典データセット | uspto-grants-1985_07 |
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| ORD ID | ord-edebad08f5b148ccac7479e949a5f540 |
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| 出典メモ | uspto-grants-1985_07 |
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