関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Butyl methanesulfonate | HCID 15953 | — |
| 反応物 | Butyl Stearate | HCID 31278 | — |
| 反応物 | Potassium Stearate | HCID 23673840 | — |
| 生成物 | Butyl Stearate | HCID 31278 | — |
| 生成物 | Potassium mesylate | HCID 23666501 | — |
反応手順
An esterification reaction mixture (94 g), consisting of butanol (ca., 4.9% w/w), butyl stearate (95.1% w/w), residual stearic acid (trace), residual methanesulfonic acid catalyst (1383 ppm) and undesired butyl methanesulfonate (613 ppm) was treated with 45% aqueous KOH (229 mg, 1.84 mmol as compared to 1.74 mmol MSA originally charged to the reaction). The resulting mixture was heating at 50° C. for 40 minutes. Without wishing to be bound by any particular theory or explanation, it is believed that reaction of butyl stearate with KOH produced potassium stearate, which retains significant solubility in the butyl stearate medium. The formed potassium stearate then reacted with butyl methanesulfonate to produce potassium methanesulfonate and butyl stearate. After filtration of the by-product solid salts (0.6325 g), analysis of the mixture by gas chromatography revealed only 300 ppm unreacted butyl methanesulfonate, a 51% reduction.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07297813B2 |
|---|
| 出典データセット | uspto-grants-2007_11 |
|---|
| ORD ID | ord-10d5384285bd45ec8ec72b7fe6287bbb |
|---|
| 出典メモ | uspto-grants-2007_11 |
|---|