참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,2-Octadecanediol | HCID 89314 | — |
| 반응물 | Dimethyl ester phosphorous acid | HCID 94853 | — |
| 반응물 | 1,2-Hexadecanediol | HCID 98037 | — |
| 반응물 | Pentadecane-1,2-diol | HCID 118123 | — |
| 반응물 | 1,2-Heptadecanediol | HCID 3015706 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | Pentadecanediol Octadecanediol | HCID 86740139 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04532057 |
|---|
| 출처 데이터셋 | uspto-grants-1985_07 |
|---|
| ORD ID | ord-edebad08f5b148ccac7479e949a5f540 |
|---|
| 출처 메모 | uspto-grants-1985_07 |
|---|