関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 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 | — |
| 反応物 | Octadecanediol | HCID 20562952 | — |
| 反応物 | Dimethylphosphite | HCID 21884954 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Pentadecanediol Octadecanediol | HCID 86740139 | — |
反応手順
Approximately 360 g of 1,2-mixed pentadecanediol to octadecanediol (commercially obtained as Vikol 158 from Viking Chemical Co. and containing about 28% 1,2-pentadecanediol, about 28% 1,2-hexadecanediol, about 28% 1,2-heptadecanediol and about 16% octadecanediol, all percentages by weight) are 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 the solids and 55 g of dimethyl 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. Methanol was observed forming and collecting in the trap. The crude product was vacuum stripped at 150° C. to remove volatile materials, producing 375 g of intermediate additive. The intermediate was an amber fluid which became waxy after cooling.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US04555353 |
|---|
| 出典データセット | uspto-grants-1985_11 |
|---|
| ORD ID | ord-1e15ba772b424052b21729cd74744121 |
|---|
| 出典メモ | uspto-grants-1985_11 |
|---|